ClinVar Miner

List of variants in gene TRPM6 reported as likely benign for abdominal and pelvic region disorder

Included ClinVar conditions (1030):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 17
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HGVS dbSNP
NM_017662.4(TRPM6):c.-163A>G rs73538241
NM_017662.4(TRPM6):c.-167A>C rs77048628
NM_017662.5(TRPM6):c.*1160C>T
NM_017662.5(TRPM6):c.*1222C>T rs190131362
NM_017662.5(TRPM6):c.*1784A>G
NM_017662.5(TRPM6):c.*235C>T
NM_017662.5(TRPM6):c.*670A>C
NM_017662.5(TRPM6):c.*710_*711AT[3] rs201267884
NM_017662.5(TRPM6):c.*919G>T
NM_017662.5(TRPM6):c.*96C>G
NM_017662.5(TRPM6):c.1014G>T (p.Met338Ile) rs56155062
NM_017662.5(TRPM6):c.2428C>T (p.Leu810=) rs55956641
NM_017662.5(TRPM6):c.2649T>C (p.Ala883=) rs373991938
NM_017662.5(TRPM6):c.4569A>T (p.Thr1523=) rs150409948
NM_017662.5(TRPM6):c.511G>A (p.Gly171Arg) rs150874152
NM_017662.5(TRPM6):c.622C>A (p.Pro208Thr)
NM_017662.5(TRPM6):c.633T>C (p.Gly211=) rs144221623

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