ClinVar Miner

List of variants in gene B9D1 reported as uncertain significance for abdominal and pelvic region disorder

Included ClinVar conditions (902):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 11
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HGVS dbSNP
NM_001243473.2(B9D1):c.74C>G (p.Ser25Cys) rs529182605
NM_015681.5(B9D1):c.*47C>T rs200124070
NM_015681.5(B9D1):c.109G>A (p.Gly37Ser) rs771997194
NM_015681.5(B9D1):c.151T>C (p.Ser51Pro)
NM_015681.5(B9D1):c.285C>A (p.Phe95Leu) rs373478202
NM_015681.5(B9D1):c.376T>A (p.Ser126Thr) rs201299216
NM_015681.5(B9D1):c.434C>T (p.Thr145Ile) rs765607415
NM_015681.5(B9D1):c.457G>A (p.Gly153Ser) rs372249324
NM_015681.5(B9D1):c.467G>C (p.Arg156Pro) rs886038205
NM_015681.5(B9D1):c.580T>C (p.Leu194=) rs7212549
NM_015681.5(B9D1):c.90C>T (p.Cys30=) rs886052685

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