rs193922491

Orientation

minus

Stabilized

minus

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

Make rs193922491(C;T)

Make rs193922491(T;T)

Reference

GRCh38 38.1/141

Chromosome

17

Position

37733663

Gene

HNF1B

is a	snp
is	mentioned by
dbSNP	rs193922491
dbSNP (classic)	rs193922491
ClinGen	rs193922491
ebi	rs193922491
HLI	rs193922491
Exac	rs193922491
Gnomad	rs193922491
Varsome	rs193922491
LitVar	rs193922491
Map	rs193922491
PheGenI	rs193922491
Biobank	rs193922491
1000 genomes	rs193922491
hgdp	rs193922491
ensembl	rs193922491
geneview	rs193922491
scholar	rs193922491
google	rs193922491
pharmgkb	rs193922491
gwascentral	rs193922491
openSNP	rs193922491
23andMe	rs193922491
SNPshot	rs193922491
SNPdbe	rs193922491
MSV3d	rs193922491
GWAS Ctlg	rs193922491

Max Magnitude

0

ClinVar
Risk	rs193922491(T;T)
Alt	rs193922491(T;T)
Reference	Rs193922491(C;C)
Significance	Probable-Pathogenic
Disease	Familial hypoplastic
Variation	info
Gene	HNF1B
CLNDBN	Familial hypoplastic, glomerulocystic kidney
Reversed	1
HGVS	NC_000017.10:g.36093656G>A
CLNSRC	ClinVar LabCorp
CLNACC	RCV000030532.1,