ClinVar Miner

List of variants in gene GLMN reported as benign for cardiovascular disorder

Included ClinVar conditions (1426):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 25
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HGVS dbSNP gnomAD frequency
NM_053274.3(GLMN):c.*115G>C rs2046620 0.45929
NM_053274.3(GLMN):c.977+7T>A rs61758979 0.01597
NM_053274.3(GLMN):c.1007T>C (p.Leu336Ser) rs35258161 0.01163
NM_053274.3(GLMN):c.1159A>G (p.Met387Val) rs78101774 0.00770
NM_053274.3(GLMN):c.-54T>G rs145401012 0.00744
NM_053274.3(GLMN):c.436G>A (p.Ala146Thr) rs61754623 0.00445
NM_053274.3(GLMN):c.165+10A>G rs201467961 0.00226
NM_053274.3(GLMN):c.519T>C (p.Leu173=) rs146069171 0.00193
NM_053274.3(GLMN):c.271G>A (p.Asp91Asn) rs144577963 0.00115
NM_053274.3(GLMN):c.1057T>C (p.Tyr353His) rs149792649 0.00098
NM_053274.3(GLMN):c.1099-4C>T rs200121766 0.00095
NM_053274.3(GLMN):c.977+9G>A rs142642620 0.00084
NM_053274.3(GLMN):c.899T>C (p.Ile300Thr) rs34062020 0.00083
NM_053274.3(GLMN):c.144T>G (p.Ile48Met) rs142032681 0.00060
NM_053274.3(GLMN):c.856A>G (p.Met286Val) rs139743855 0.00049
NM_053274.3(GLMN):c.58G>A (p.Asp20Asn) rs147537497 0.00042
NM_053274.3(GLMN):c.761C>G (p.Pro254Arg) rs145762716 0.00031
NM_053274.3(GLMN):c.765C>T (p.Phe255=) rs149618929 0.00021
NM_053274.3(GLMN):c.1022A>G (p.Asn341Ser) rs147889200 0.00009
NM_053274.3(GLMN):c.-34G>A rs556956035 0.00004
NM_053274.3(GLMN):c.1306C>T (p.Arg436Cys) rs188879204 0.00004
NM_053274.3(GLMN):c.1482A>T (p.Leu494Phe) rs150536401 0.00004
NM_053274.3(GLMN):c.581A>G (p.Asn194Ser) rs532530906 0.00002
NM_053274.3(GLMN):c.40-6del rs372630078
NM_053274.3(GLMN):c.542T>C (p.Ile181Thr) rs139873200

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