rs193922493

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(A;A)	0	common in clinvar

Make rs193922493(A;G)

Make rs193922493(G;G)

Reference

GRCh38 38.1/141

Chromosome

17

Position

37731678

Gene

HNF1B

is a	snp
is	mentioned by
dbSNP	rs193922493
dbSNP (classic)	rs193922493
ClinGen	rs193922493
ebi	rs193922493
HLI	rs193922493
Exac	rs193922493
Gnomad	rs193922493
Varsome	rs193922493
LitVar	rs193922493
Map	rs193922493
PheGenI	rs193922493
Biobank	rs193922493
1000 genomes	rs193922493
hgdp	rs193922493
ensembl	rs193922493
geneview	rs193922493
scholar	rs193922493
google	rs193922493
pharmgkb	rs193922493
gwascentral	rs193922493
openSNP	rs193922493
23andMe	rs193922493
SNPshot	rs193922493
SNPdbe	rs193922493
MSV3d	rs193922493
GWAS Ctlg	rs193922493

Max Magnitude

0

ClinVar
Risk	rs193922493(G;G)
Alt	rs193922493(G;G)
Reference	Rs193922493(A;A)
Significance	Probable-Pathogenic
Disease	Familial hypoplastic
Variation	info
Gene	HNF1B
CLNDBN	Familial hypoplastic, glomerulocystic kidney
Reversed	1
HGVS	NC_000017.10:g.36091669T>C
CLNSRC	ClinVar LabCorp
CLNACC	RCV000030537.1,