ClinVar Miner

List of variants in gene LAMA4 reported as benign by Preventiongenetics, part of Exact Sciences

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Total variants: 14
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HGVS dbSNP gnomAD frequency
NM_001105206.3(LAMA4):c.3283-15C>T rs2032568 0.77184
NM_001105206.3(LAMA4):c.3349G>A (p.Gly1117Ser) rs2032567 0.77036
NM_001105206.3(LAMA4):c.1492T>C (p.Tyr498His) rs1050348 0.66129
NM_001105206.3(LAMA4):c.5160T>A (p.Val1720=) rs1050353 0.29327
NM_001105206.3(LAMA4):c.651C>T (p.Thr217=) rs2072021 0.26664
NM_001105206.3(LAMA4):c.5326+6T>G rs3734289 0.24973
NM_001105206.3(LAMA4):c.5326+15A>C rs3734290 0.24942
NM_001105206.3(LAMA4):c.3356C>G (p.Pro1119Arg) rs1050349 0.21500
NM_001105206.3(LAMA4):c.1710T>C (p.Ser570=) rs3752577 0.08618
NM_001105206.3(LAMA4):c.1357+4G>T rs6917763 0.07821
NM_001105206.3(LAMA4):c.4716C>T (p.Leu1572=) rs35679345 0.06874
NM_001105206.3(LAMA4):c.460C>T (p.Arg154Trp) rs11757455 0.04245
NM_001105206.3(LAMA4):c.1190-8C>G rs73538515 0.03405
NM_001105206.3(LAMA4):c.3239G>A (p.Arg1080Gln) rs41289902 0.01045

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