ClinVar Miner

List of variants in gene HNF1B reported as likely benign 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: 20
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HGVS dbSNP
NM_000458.3(HNF1B):c.-178G>A rs148442901
NM_000458.3(HNF1B):c.-232C>T rs142612536
NM_000458.4(HNF1B):c.*403A>G rs557216745
NM_000458.4(HNF1B):c.*445A>G rs571607314
NM_000458.4(HNF1B):c.*683G>A rs144234352
NM_000458.4(HNF1B):c.*804T>C rs75361710
NM_000458.4(HNF1B):c.*938A>G rs574000398
NM_000458.4(HNF1B):c.-67C>T rs140699244
NM_000458.4(HNF1B):c.1045+12T>C rs141166864
NM_000458.4(HNF1B):c.1413C>T (p.Pro471=) rs140781855
NM_000458.4(HNF1B):c.1474G>A (p.Gly492Ser) rs187556368
NM_000458.4(HNF1B):c.226G>T (p.Gly76Cys) rs144425830
NM_000458.4(HNF1B):c.244G>A (p.Asp82Asn) rs140562402
NM_000458.4(HNF1B):c.444G>A (p.Ser148=) rs147218489
NM_000458.4(HNF1B):c.684C>G (p.Asn228Lys) rs202151409
NM_000458.4(HNF1B):c.708C>T (p.Phe236=)
NM_000458.4(HNF1B):c.73G>T (p.Val25Leu) rs139107479
NM_000458.4(HNF1B):c.750C>T (p.Tyr250=) rs144249535
NM_000458.4(HNF1B):c.810-4C>G
NM_000458.4(HNF1B):c.951C>G (p.Ala317=) rs145750370

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