ClinVar Miner

List of variants in gene LAMA1 reported as benign by Invitae

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Gene type:
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Total variants: 134
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HGVS dbSNP gnomAD frequency
NM_005559.4(LAMA1):c.5380-13G>A rs617573 0.82747
NM_005559.4(LAMA1):c.5496+20A>G rs616722 0.82650
NM_005559.4(LAMA1):c.6004A>G (p.Lys2002Glu) rs607230 0.68054
NM_005559.4(LAMA1):c.2763T>C (p.Cys921=) rs539713 0.61217
NM_005559.4(LAMA1):c.3378T>C (p.Gly1126=) rs9946794 0.48883
NM_005559.4(LAMA1):c.2493T>C (p.Cys831=) rs684634 0.48817
NM_005559.4(LAMA1):c.5391G>A (p.Leu1797=) rs617206 0.48492
NM_005559.4(LAMA1):c.5496+19C>T rs523711 0.48483
NM_005559.4(LAMA1):c.2109C>T (p.Ala703=) rs621993 0.46872
NM_005559.4(LAMA1):c.2051+14A>T rs674733 0.46819
NM_005559.4(LAMA1):c.8844+19T>G rs2155697 0.42907
NM_005559.4(LAMA1):c.3573C>T (p.Thr1191=) rs619106 0.39038
NM_005559.4(LAMA1):c.6227T>C (p.Ile2076Thr) rs671871 0.29406
NM_005559.4(LAMA1):c.4018A>G (p.Met1340Val) rs662471 0.26135
NM_005559.4(LAMA1):c.3126+7A>G rs603258 0.25992
NM_005559.4(LAMA1):c.8982C>T (p.Asp2994=) rs2016639 0.25393
NM_005559.4(LAMA1):c.4729T>G (p.Ser1577Ala) rs12961939 0.21927
NM_005559.4(LAMA1):c.2021A>C (p.Asn674Thr) rs566655 0.20323
NM_005559.4(LAMA1):c.5256C>T (p.His1752=) rs62081531 0.17890
NM_005559.4(LAMA1):c.4026T>G (p.Val1342=) rs73938538 0.15758
NM_005559.4(LAMA1):c.4975A>G (p.Ile1659Val) rs62081533 0.15549
NM_005559.4(LAMA1):c.5288C>T (p.Ala1763Val) rs12607841 0.13777
NM_005559.4(LAMA1):c.6345+7T>C rs10164200 0.12418
NM_005559.4(LAMA1):c.4416C>T (p.His1472=) rs12970643 0.10317
NM_005559.4(LAMA1):c.6040C>T (p.Leu2014=) rs9955616 0.08747
NM_005559.4(LAMA1):c.3508-12T>C rs61695598 0.08121
NM_005559.4(LAMA1):c.1046T>C (p.Leu349Ser) rs9950267 0.05935
NM_005559.4(LAMA1):c.6900C>T (p.Ser2300=) rs73390557 0.04975
NM_005559.4(LAMA1):c.6819G>A (p.Gly2273=) rs615809 0.04108
NM_005559.4(LAMA1):c.7050+16C>T rs9956659 0.03677
NM_005559.4(LAMA1):c.3648G>A (p.Pro1216=) rs12969598 0.03504
NM_005559.4(LAMA1):c.5700C>A (p.Thr1900=) rs11661974 0.02811
NM_005559.4(LAMA1):c.7474C>T (p.Leu2492=) rs73390547 0.02637
NM_005559.4(LAMA1):c.8736A>G (p.Ser2912=) rs78279255 0.02505
NM_005559.4(LAMA1):c.7143T>C (p.Arg2381=) rs16950892 0.02310
NM_005559.4(LAMA1):c.5045A>T (p.Asp1682Val) rs16950981 0.02255
NM_005559.4(LAMA1):c.3171T>C (p.Asp1057=) rs9953287 0.02080
NM_005559.4(LAMA1):c.3615C>T (p.Ala1205=) rs79497917 0.01899
NM_005559.4(LAMA1):c.3402G>T (p.Glu1134Asp) rs113553100 0.01725
NM_005559.4(LAMA1):c.7531C>A (p.Leu2511Met) rs60009920 0.01514
NM_005559.4(LAMA1):c.6430C>G (p.Leu2144Val) rs117225191 0.01415
NM_005559.4(LAMA1):c.1300A>G (p.Thr434Ala) rs62619829 0.01374
NM_005559.4(LAMA1):c.3180C>T (p.Thr1060=) rs34712919 0.01365
NM_005559.4(LAMA1):c.2490-16T>C rs113838739 0.01255
NM_005559.4(LAMA1):c.2349G>T (p.Gly783=) rs28687669 0.01247
NM_005559.4(LAMA1):c.4894A>G (p.Lys1632Glu) rs11872364 0.01195
NM_005559.4(LAMA1):c.1675G>A (p.Val559Ile) rs16951079 0.01121
NM_005559.4(LAMA1):c.434C>T (p.Thr145Met) rs77811721 0.00953
NM_005559.4(LAMA1):c.3156T>C (p.Thr1052=) rs115609096 0.00929
NM_005559.4(LAMA1):c.1839+13G>A rs143604947 0.00895
NM_005559.4(LAMA1):c.768+13C>T rs111413671 0.00830
NM_005559.4(LAMA1):c.7963G>C (p.Glu2655Gln) rs73390524 0.00804
NM_005559.4(LAMA1):c.1803C>T (p.Asp601=) rs111267165 0.00759
NM_005559.4(LAMA1):c.674G>A (p.Arg225His) rs140718292 0.00690
NM_005559.4(LAMA1):c.6535C>T (p.Leu2179=) rs115169112 0.00689
NM_005559.4(LAMA1):c.8557-17C>T rs115493936 0.00601
NM_005559.4(LAMA1):c.8454T>C (p.Ser2818=) rs145580032 0.00598
NM_005559.4(LAMA1):c.8398-13C>T rs142663020 0.00594
NM_005559.4(LAMA1):c.8403G>A (p.Lys2801=) rs147737122 0.00593
NM_005559.4(LAMA1):c.8903C>T (p.Thr2968Ile) rs202107482 0.00514
NM_005559.4(LAMA1):c.6850C>T (p.Leu2284=) rs77810945 0.00458
NM_005559.4(LAMA1):c.6883C>T (p.Arg2295Cys) rs76842111 0.00458
NM_005559.4(LAMA1):c.7051-8T>G rs150737889 0.00403
NM_005559.4(LAMA1):c.1673C>T (p.Ala558Val) rs143997842 0.00351
NM_005559.4(LAMA1):c.3294G>A (p.Ser1098=) rs149157836 0.00322
NM_005559.4(LAMA1):c.9067+4T>C rs8091658 0.00303
NM_005559.4(LAMA1):c.2299G>A (p.Val767Ile) rs149611371 0.00302
NM_005559.4(LAMA1):c.5302G>A (p.Val1768Met) rs73938527 0.00297
NM_005559.4(LAMA1):c.2052-18C>A rs139216533 0.00293
NM_005559.4(LAMA1):c.1183C>T (p.Arg395Cys) rs148751644 0.00282
NM_005559.4(LAMA1):c.8253G>A (p.Leu2751=) rs139713073 0.00271
NM_005559.4(LAMA1):c.3559T>C (p.Leu1187=) rs141269552 0.00230
NM_005559.4(LAMA1):c.2657C>T (p.Ala886Val) rs144738522 0.00225
NM_005559.4(LAMA1):c.2186G>A (p.Arg729His) rs144429570 0.00222
NM_005559.4(LAMA1):c.2814C>T (p.Gly938=) rs77574121 0.00207
NM_005559.4(LAMA1):c.5481A>G (p.Val1827=) rs138711280 0.00201
NM_005559.4(LAMA1):c.6840A>G (p.Lys2280=) rs113914459 0.00196
NM_005559.4(LAMA1):c.3946G>A (p.Asp1316Asn) rs149753863 0.00183
NM_005559.4(LAMA1):c.6354C>T (p.Val2118=) rs150849018 0.00180
NM_005559.4(LAMA1):c.4554C>T (p.His1518=) rs145068849 0.00176
NM_005559.4(LAMA1):c.2900G>A (p.Gly967Asp) rs141851670 0.00161
NM_005559.4(LAMA1):c.5660+7A>G rs144775658 0.00157
NM_005559.4(LAMA1):c.4692G>A (p.Leu1564=) rs147374927 0.00150
NM_005559.4(LAMA1):c.4540C>T (p.His1514Tyr) rs140577242 0.00148
NM_005559.4(LAMA1):c.7446A>G (p.Leu2482=) rs145257845 0.00144
NM_005559.4(LAMA1):c.665G>A (p.Arg222Gln) rs112194576 0.00142
NM_005559.4(LAMA1):c.5867A>G (p.Asn1956Ser) rs117433399 0.00136
NM_005559.4(LAMA1):c.977-19G>A rs201749821 0.00131
NM_005559.4(LAMA1):c.3363+9C>T rs200796194 0.00130
NM_005559.4(LAMA1):c.1716C>T (p.Pro572=) rs144105602 0.00118
NM_005559.4(LAMA1):c.4461C>T (p.His1487=) rs143389887 0.00118
NM_005559.4(LAMA1):c.6066G>A (p.Ala2022=) rs150951157 0.00101
NM_005559.4(LAMA1):c.2164-4G>A rs185519807 0.00087
NM_005559.4(LAMA1):c.7338-8C>T rs377116281 0.00072
NM_005559.4(LAMA1):c.4878G>A (p.Thr1626=) rs763453529 0.00066
NM_005559.4(LAMA1):c.3145G>A (p.Val1049Met) rs138476816 0.00059
NM_005559.4(LAMA1):c.1738-15G>A rs181427766 0.00047
NM_005559.4(LAMA1):c.3522C>T (p.Ser1174=) rs139418084 0.00045
NM_005559.4(LAMA1):c.6801T>C (p.His2267=) rs200986684 0.00024
NM_005559.4(LAMA1):c.53G>A (p.Arg18Gln) rs182087823 0.00023
NM_005559.4(LAMA1):c.8447G>A (p.Arg2816Gln) rs200996196 0.00019
NM_005559.4(LAMA1):c.8631G>A (p.Val2877=) rs372751048 0.00017
NM_005559.4(LAMA1):c.2136G>T (p.Pro712=) rs139988519 0.00016
NM_005559.4(LAMA1):c.435G>A (p.Thr145=) rs200618216 0.00016
NM_005559.4(LAMA1):c.9067+8C>T rs202100640 0.00015
NM_005559.4(LAMA1):c.5960C>T (p.Thr1987Ile) rs117303816 0.00009
NM_005559.4(LAMA1):c.3256G>A (p.Asp1086Asn) rs201831309 0.00007
NM_005559.4(LAMA1):c.5983T>C (p.Leu1995=) rs775719349 0.00007
NM_005559.4(LAMA1):c.5832C>T (p.Ala1944=) rs530014646 0.00006
NM_005559.4(LAMA1):c.1784T>C (p.Ile595Thr) rs374756793 0.00004
NM_005559.4(LAMA1):c.4618G>A (p.Asp1540Asn) rs373453681 0.00004
NM_005559.4(LAMA1):c.465C>T (p.Ser155=) rs192198427 0.00004
NM_005559.4(LAMA1):c.6553G>A (p.Gly2185Arg) rs773262827 0.00004
NM_005559.4(LAMA1):c.7875C>T (p.Val2625=) rs114578861 0.00004
NM_005559.4(LAMA1):c.8315G>A (p.Arg2772His) rs548903685 0.00002
NM_005559.4(LAMA1):c.4735A>G (p.Asn1579Asp) rs542801679 0.00001
NM_005559.4(LAMA1):c.6900-11C>G rs776544976 0.00001
NM_005559.4(LAMA1):c.120C>T (p.Thr40=)
NM_005559.4(LAMA1):c.2052-18_2052-16del rs559173743
NM_005559.4(LAMA1):c.2701+15G>A rs74986202
NM_005559.4(LAMA1):c.2784T>C (p.Thr928=) rs199655492
NM_005559.4(LAMA1):c.2809-14dup rs2144126881
NM_005559.4(LAMA1):c.3215G>T (p.Arg1072Leu) rs118089415
NM_005559.4(LAMA1):c.3688-19_3688-17del rs535197995
NM_005559.4(LAMA1):c.4066G>A (p.Ala1356Thr)
NM_005559.4(LAMA1):c.4479A>G (p.Ser1493=) rs625106
NM_005559.4(LAMA1):c.5626G>A (p.Ala1876Thr) rs11664063
NM_005559.4(LAMA1):c.5891-15dup
NM_005559.4(LAMA1):c.6346-12T>C rs182927027
NM_005559.4(LAMA1):c.7337+16G>T
NM_005559.4(LAMA1):c.7453-19C>T rs9964082
NM_005559.4(LAMA1):c.7831A>C (p.Thr2611Pro) rs543355
NM_005559.4(LAMA1):c.7831A>G (p.Thr2611Ala) rs543355
NM_005559.4(LAMA1):c.9018G>A (p.Gln3006=)

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