rs193922487

Orientation

minus

Stabilized

minus

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

Make rs193922487(A;A)

Make rs193922487(A;G)

Reference

GRCh38 38.1/141

Chromosome

17

Position

37744541

Gene

HNF1B

is a	snp
is	mentioned by
dbSNP	rs193922487
dbSNP (classic)	rs193922487
ClinGen	rs193922487
ebi	rs193922487
HLI	rs193922487
Exac	rs193922487
Gnomad	rs193922487
Varsome	rs193922487
LitVar	rs193922487
Map	rs193922487
PheGenI	rs193922487
Biobank	rs193922487
1000 genomes	rs193922487
hgdp	rs193922487
ensembl	rs193922487
geneview	rs193922487
scholar	rs193922487
google	rs193922487
pharmgkb	rs193922487
gwascentral	rs193922487
openSNP	rs193922487
23andMe	rs193922487
SNPshot	rs193922487
SNPdbe	rs193922487
MSV3d	rs193922487
GWAS Ctlg	rs193922487

Max Magnitude

0

ClinVar
Risk	rs193922487(A;A)
Alt	rs193922487(A;A)
Reference	Rs193922487(G;G)
Significance	Probable-Pathogenic
Disease	Familial hypoplastic
Variation	info
Gene	HNF1B
CLNDBN	Familial hypoplastic, glomerulocystic kidney
Reversed	1
HGVS	NC_000017.10:g.36104532C>T
CLNSRC	ClinVar LabCorp
CLNACC	RCV000030527.1,