ClinVar Miner

List of variants in gene FREM1 reported as benign by Invitae

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Gene type:
ClinVar version:
Total variants: 83
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HGVS dbSNP gnomAD frequency
NM_001379081.2(FREM1):c.4791T>C (p.Asp1597=) rs1032474 0.85601
NM_001379081.2(FREM1):c.6428A>C (p.Gln2143Pro) rs10961689 0.74114
NM_001379081.2(FREM1):c.829-12A>G rs2818940 0.72914
NM_001379081.2(FREM1):c.1315G>C (p.Val439Leu) rs2779500 0.56393
NM_001379081.2(FREM1):c.4785C>T (p.Ala1595=) rs10733289 0.50486
NM_001379081.2(FREM1):c.5004C>A (p.Ile1668=) rs17219005 0.34768
NM_001379081.2(FREM1):c.3634G>T (p.Ala1212Ser) rs35870000 0.27977
NM_001379081.2(FREM1):c.4857+8T>C rs1874108 0.19884
NM_001379081.2(FREM1):c.2408C>A (p.Ser803Tyr) rs7023244 0.19696
NM_001379081.2(FREM1):c.3089-4G>T rs10810249 0.18577
NM_001379081.2(FREM1):c.456A>G (p.Gln152=) rs10961757 0.17917
NM_001379081.2(FREM1):c.3657A>G (p.Ala1219=) rs10738380 0.17766
NM_001379081.2(FREM1):c.3606C>G (p.Ser1202Arg) rs16932300 0.15197
NM_001379081.2(FREM1):c.4617G>A (p.Ala1539=) rs2131880 0.14595
NM_001379081.2(FREM1):c.5859T>C (p.Val1953=) rs4741426 0.14468
NM_001379081.2(FREM1):c.2073C>T (p.Ser691=) rs12236053 0.13982
NM_001379081.2(FREM1):c.2587C>G (p.Leu863Val) rs7041710 0.12780
NM_001379081.2(FREM1):c.4504G>A (p.Val1502Met) rs10961700 0.11621
NM_001379081.2(FREM1):c.639A>G (p.Arg213=) rs950739 0.09339
NM_001379081.2(FREM1):c.1495A>G (p.Ile499Val) rs1353223 0.08593
NM_001379081.2(FREM1):c.3471+11T>C rs72614223 0.06395
NM_001379081.2(FREM1):c.4421C>T (p.Thr1474Ile) rs41265306 0.06329
NM_001379081.2(FREM1):c.3819T>A (p.Asp1273Glu) rs7025814 0.06135
NM_001379081.2(FREM1):c.2277T>C (p.Gly759=) rs16932323 0.03898
NM_001379081.2(FREM1):c.2104A>G (p.Met702Val) rs7864984 0.03461
NM_001379081.2(FREM1):c.273T>C (p.Tyr91=) rs61740262 0.02932
NM_001379081.2(FREM1):c.3048G>A (p.Thr1016=) rs61732546 0.02603
NM_001379081.2(FREM1):c.840G>A (p.Ala280=) rs41313784 0.02530
NM_001379081.2(FREM1):c.6255-4T>G rs75897613 0.01885
NM_001379081.2(FREM1):c.3708G>A (p.Thr1236=) rs61747541 0.01749
NM_001379081.2(FREM1):c.1512C>T (p.His504=) rs61735720 0.01644
NM_001379081.2(FREM1):c.4466G>A (p.Arg1489Gln) rs61732355 0.01493
NM_001379081.2(FREM1):c.2358A>G (p.Lys786=) rs61745880 0.01483
NM_001379081.2(FREM1):c.5814T>A (p.Val1938=) rs114909107 0.01236
NM_001379081.2(FREM1):c.3472-20T>C rs77508679 0.01216
NM_001379081.2(FREM1):c.1791T>C (p.Tyr597=) rs115032700 0.01114
NM_001379081.2(FREM1):c.1047G>A (p.Leu349=) rs115701214 0.00859
NM_001379081.2(FREM1):c.4727A>T (p.Asn1576Ile) rs2101770 0.00620
NM_001379081.2(FREM1):c.5466T>C (p.Asp1822=) rs61741992 0.00569
NM_001379081.2(FREM1):c.3575G>A (p.Arg1192His) rs79023327 0.00551
NM_001379081.2(FREM1):c.45G>T (p.Leu15=) rs61747529 0.00547
NM_001379081.2(FREM1):c.3478G>A (p.Glu1160Lys) rs145337987 0.00502
NM_001379081.2(FREM1):c.2274C>A (p.Gly758=) rs12235714 0.00497
NM_001379081.2(FREM1):c.635T>G (p.Leu212Arg) rs145369669 0.00451
NM_001379081.2(FREM1):c.1884G>A (p.Val628=) rs140144319 0.00405
NM_001379081.2(FREM1):c.5329A>G (p.Ile1777Val) rs73644847 0.00380
NM_001379081.2(FREM1):c.4377T>C (p.Asp1459=) rs148327330 0.00362
NM_001379081.2(FREM1):c.6528C>T (p.Ser2176=) rs144454947 0.00247
NM_001379081.2(FREM1):c.2337+19A>G rs201898982 0.00158
NM_001379081.2(FREM1):c.1464C>T (p.Ser488=) rs200064797 0.00155
NM_001379081.2(FREM1):c.5205-14C>T rs77061232 0.00153
NM_001379081.2(FREM1):c.6258C>T (p.Tyr2086=) rs187325866 0.00119
NM_001379081.2(FREM1):c.3147C>T (p.Ser1049=) rs200894045 0.00092
NM_001379081.2(FREM1):c.5049C>T (p.Asn1683=) rs200063334 0.00089
NM_001379081.2(FREM1):c.3359A>T (p.Gln1120Leu) rs143844459 0.00068
NM_001379081.2(FREM1):c.4875A>C (p.Lys1625Asn) rs117881664 0.00033
NM_001379081.2(FREM1):c.6279A>G (p.Val2093=) rs373107801 0.00033
NM_001379081.2(FREM1):c.4859T>C (p.Val1620Ala) rs190763692 0.00029
NM_001379081.2(FREM1):c.4941C>T (p.Tyr1647=) rs373880888 0.00020
NM_001379081.2(FREM1):c.2601C>T (p.Thr867=) rs369150540 0.00019
NM_001379081.2(FREM1):c.1329C>T (p.Asp443=) rs201393312 0.00009
NM_001379081.2(FREM1):c.571G>A (p.Gly191Arg) rs370556388 0.00009
NM_001379081.2(FREM1):c.1739-17T>C rs191993020 0.00008
NM_001379081.2(FREM1):c.1492C>T (p.Arg498Trp) rs200642807 0.00006
NM_001379081.2(FREM1):c.4754A>G (p.Asp1585Gly) rs544905717 0.00001
NM_001379081.2(FREM1):c.1394G>C (p.Gly465Ala) rs41298151
NM_001379081.2(FREM1):c.2078+11del
NM_001379081.2(FREM1):c.3274+15C>T
NM_001379081.2(FREM1):c.3330G>A (p.Arg1110=)
NM_001379081.2(FREM1):c.3517G>T (p.Ala1173Ser) rs564039071
NM_001379081.2(FREM1):c.3717TGA[1] (p.Asp1241del)
NM_001379081.2(FREM1):c.3840-10C>G
NM_001379081.2(FREM1):c.4244C>G (p.Thr1415Ser) rs75677527
NM_001379081.2(FREM1):c.4563C>A (p.Ala1521=) rs60091943
NM_001379081.2(FREM1):c.459G>T (p.Ala153=)
NM_001379081.2(FREM1):c.516C>T (p.Thr172=) rs41265310
NM_001379081.2(FREM1):c.5335-11del rs140882884
NM_001379081.2(FREM1):c.5335-11dup rs140882884
NM_001379081.2(FREM1):c.5335-8dup rs201316684
NM_001379081.2(FREM1):c.5408-17del
NM_001379081.2(FREM1):c.6139-4T>A rs77135480
NM_001379081.2(FREM1):c.6139-4T>C rs77135480
NM_001379081.2(FREM1):c.6474G>A (p.Gly2158=)

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