ClinVar Miner

List of variants in gene LAMB2 reported as uncertain significance for not provided

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Total variants: 47
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HGVS dbSNP gnomAD frequency
NM_002292.4(LAMB2):c.1306G>A (p.Gly436Ser) rs142402808 0.00096
NM_002292.4(LAMB2):c.4118A>G (p.Asp1373Gly) rs112933248 0.00076
NM_002292.4(LAMB2):c.703C>T (p.Arg235Trp) rs144133177 0.00071
NM_002292.4(LAMB2):c.598G>A (p.Val200Ile) rs149325182 0.00034
NM_002292.4(LAMB2):c.5039C>T (p.Ala1680Val) rs141473691 0.00033
NM_002292.4(LAMB2):c.4304C>T (p.Pro1435Leu) rs140968382 0.00032
NM_002292.4(LAMB2):c.1762C>G (p.Pro588Ala) rs144324168 0.00026
NM_002292.4(LAMB2):c.101C>A (p.Ala34Asp) rs202057459 0.00024
NM_002292.4(LAMB2):c.2271C>A (p.Ser757Arg) rs143405268 0.00021
NM_002292.4(LAMB2):c.5233G>A (p.Ala1745Thr) rs142041381 0.00021
NM_002292.4(LAMB2):c.253G>A (p.Glu85Lys) rs140371771 0.00020
NM_002292.4(LAMB2):c.3674G>A (p.Gly1225Asp) rs150013302 0.00019
NM_002292.4(LAMB2):c.5379C>G (p.Ile1793Met) rs11550620 0.00019
NM_002292.4(LAMB2):c.914T>C (p.Met305Thr) rs199794467 0.00019
NM_002292.4(LAMB2):c.4148A>G (p.His1383Arg) rs754983373 0.00014
NM_002292.4(LAMB2):c.1442G>A (p.Ser481Asn) rs144230655 0.00012
NM_002292.4(LAMB2):c.2167C>T (p.Arg723Cys) rs145660751 0.00010
NM_002292.4(LAMB2):c.2639A>G (p.Asn880Ser) rs781619412 0.00009
NM_002292.4(LAMB2):c.2983A>G (p.Met995Val) rs773681564 0.00006
NM_002292.4(LAMB2):c.800G>A (p.Arg267Gln) rs772368832 0.00006
NM_002292.4(LAMB2):c.1015G>A (p.Gly339Ser) rs376294474 0.00004
NM_002292.4(LAMB2):c.2089C>T (p.Arg697Trp) rs149304508 0.00004
NM_002292.4(LAMB2):c.4001G>C (p.Arg1334Pro) rs144783830 0.00004
NM_002292.4(LAMB2):c.2219G>A (p.Arg740His) rs781721930 0.00003
NM_002292.4(LAMB2):c.249+1G>A rs779317615 0.00003
NM_002292.4(LAMB2):c.646G>A (p.Glu216Lys) rs368339529 0.00003
NM_002292.4(LAMB2):c.1518+5G>A rs768311062 0.00002
NM_002292.4(LAMB2):c.1981G>A (p.Asp661Asn) rs1424372955 0.00001
NM_002292.4(LAMB2):c.2669C>T (p.Thr890Ile) rs527639885 0.00001
NM_002292.4(LAMB2):c.2726T>C (p.Ile909Thr) rs201756319 0.00001
NM_002292.4(LAMB2):c.3287C>A (p.Ala1096Asp) rs746590503 0.00001
NM_002292.4(LAMB2):c.4227G>A (p.Val1409=) rs766376770 0.00001
NM_002292.4(LAMB2):c.4676T>C (p.Ile1559Thr) rs748097623 0.00001
NM_002292.4(LAMB2):c.527G>A (p.Arg176Gln) rs924410863 0.00001
NM_002292.4(LAMB2):c.872A>G (p.Glu291Gly) rs757452525 0.00001
NM_002292.4(LAMB2):c.1087T>C (p.Tyr363His)
NM_002292.4(LAMB2):c.1390C>T (p.Arg464Cys)
NM_002292.4(LAMB2):c.1937G>A (p.Gly646Glu)
NM_002292.4(LAMB2):c.261G>C (p.Lys87Asn) rs149408554
NM_002292.4(LAMB2):c.2854A>T (p.Ile952Phe) rs146962414
NM_002292.4(LAMB2):c.364G>C (p.Ala122Pro)
NM_002292.4(LAMB2):c.3811G>A (p.Glu1271Lys) rs1560071889
NM_002292.4(LAMB2):c.4821_4822delinsGA (p.Gln1608Lys) rs1560066776
NM_002292.4(LAMB2):c.5390G>T (p.Cys1797Phe)
NM_002292.4(LAMB2):c.5394del (p.Gln1798fs)
NM_002292.4(LAMB2):c.934T>C (p.Cys312Arg) rs1057524235
NM_002292.4(LAMB2):c.970T>C (p.Cys324Arg) rs2045472442

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