rs193922492

Orientation

minus

Stabilized

minus

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

Make rs193922492(G;T)

Make rs193922492(T;T)

Reference

GRCh38 38.1/141

Chromosome

17

Position

37731691

Gene

HNF1B

is a	snp
is	mentioned by
dbSNP	rs193922492
dbSNP (classic)	rs193922492
ClinGen	rs193922492
ebi	rs193922492
HLI	rs193922492
Exac	rs193922492
Gnomad	rs193922492
Varsome	rs193922492
LitVar	rs193922492
Map	rs193922492
PheGenI	rs193922492
Biobank	rs193922492
1000 genomes	rs193922492
hgdp	rs193922492
ensembl	rs193922492
geneview	rs193922492
scholar	rs193922492
google	rs193922492
pharmgkb	rs193922492
gwascentral	rs193922492
openSNP	rs193922492
23andMe	rs193922492
SNPshot	rs193922492
SNPdbe	rs193922492
MSV3d	rs193922492
GWAS Ctlg	rs193922492

Max Magnitude

0

ClinVar
Risk	rs193922492(T;T)
Alt	rs193922492(T;T)
Reference	Rs193922492(G;G)
Significance	Probable-Pathogenic
Disease	Familial hypoplastic
Variation	info
Gene	HNF1B
CLNDBN	Familial hypoplastic, glomerulocystic kidney
Reversed	1
HGVS	NC_000017.10:g.36091682C>A
CLNSRC	ClinVar LabCorp
CLNACC	RCV000030535.1,