rs138986885

Orientation

plus

Stabilized

plus

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

Make rs138986885(C;C)

Make rs138986885(C;G)

Reference

GRCh38 38.1/141

Chromosome

17

Position

37731634

Gene

HNF1B

is a	snp
is	mentioned by
dbSNP	rs138986885
dbSNP (classic)	rs138986885
ClinGen	rs138986885
ebi	rs138986885
HLI	rs138986885
Exac	rs138986885
Gnomad	rs138986885
Varsome	rs138986885
LitVar	rs138986885
Map	rs138986885
PheGenI	rs138986885
Biobank	rs138986885
1000 genomes	rs138986885
hgdp	rs138986885
ensembl	rs138986885
geneview	rs138986885
scholar	rs138986885
google	rs138986885
pharmgkb	rs138986885
gwascentral	rs138986885
openSNP	rs138986885
23andMe	rs138986885
SNPshot	rs138986885
SNPdbe	rs138986885
MSV3d	rs138986885
GWAS Ctlg	rs138986885

Max Magnitude

0

ClinVar
Risk	rs138986885(A;A) rs138986885(C;C) rs138986885(T;T)
Alt	rs138986885(A;A) rs138986885(C;C) rs138986885(T;T)
Reference	Rs138986885(G;G)
Significance	Probable-Pathogenic
Disease	Familial hypoplastic not provided
Variation	info
Gene	HNF1B
CLNDBN	Familial hypoplastic, glomerulocystic kidney not provided
Reversed	0
HGVS	NC_000017.10:g.36091625G>A; NC_000017.10:g.36091625G>T
CLNSRC	ClinVar LabCorp
CLNACC	RCV000030518.1, RCV000421527.1,