rs587776771

Orientation

plus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common in clinvar
(CT;CT)	0	common in clinvar
(G;G)	0	common in clinvar
(I;I)	0	common genotype

Make rs587776771(-;-)

Make rs587776771(-;G)

Reference

GRCh38 38.1/142

Chromosome

17

Position

37744839

Gene

HNF1B

is a	snp
is	mentioned by
dbSNP	rs587776771
dbSNP (classic)	rs587776771
ClinGen	rs587776771
ebi	rs587776771
HLI	rs587776771
Exac	rs587776771
Gnomad	rs587776771
Varsome	rs587776771
LitVar	rs587776771
Map	rs587776771
PheGenI	rs587776771
Biobank	rs587776771
1000 genomes	rs587776771
hgdp	rs587776771
ensembl	rs587776771
geneview	rs587776771
scholar	rs587776771
google	rs587776771
pharmgkb	rs587776771
gwascentral	rs587776771
openSNP	rs587776771
23andMe	rs587776771
SNPshot	rs587776771
SNPdbe	rs587776771
MSV3d	rs587776771
GWAS Ctlg	rs587776771

Max Magnitude

0

ClinVar
Risk	Rs587776771(G;G) rs587776771(-;-)
Alt	Rs587776771(G;G) rs587776771(-;-)
Reference	Rs587776771(C;C)
Significance	Pathogenic
Disease	Chromophobe renal cell carcinoma
Variation	info
Gene	HNF1B
CLNDBN	Chromophobe renal cell carcinoma
Reversed	1
HGVS	NC_000017.10:g.36104830delG
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000013483.23,