ClinVar Miner

List of variants in gene HNF1B reported as 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: 10
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HGVS dbSNP
NM_000458.3(HNF1B):c.1654-22T>C rs3110641
NM_000458.4(HNF1B):c.*100= rs1555818000
NM_000458.4(HNF1B):c.*274= rs2689
NM_000458.4(HNF1B):c.*384A>G rs1058166
NM_000458.4(HNF1B):c.*444= rs2688
NM_000458.4(HNF1B):c.*47T>G rs8068014
NM_000458.4(HNF1B):c.*777G>A rs17138512
NM_000458.4(HNF1B):c.*924C>G rs10962
NM_000458.4(HNF1B):c.*99C>A rs2229295
NM_000458.4(HNF1B):c.345-19C>T rs59527848

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