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rs587776771

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CT;CT) 0 common in clinvar
(G;G) 0 common in clinvar
Make rs587776771(-;-)
Make rs587776771(-;G)
ReferenceGRCh38 38.1/142
Chromosome17
Position37744839
GeneHNF1B
is asnp
is mentioned by
dbSNPrs587776771
ebirs587776771
HLIrs587776771
Exacrs587776771
Varsomers587776771
Maprs587776771
PheGenIrs587776771
hapmaprs587776771
1000 genomesrs587776771
hgdprs587776771
ensemblrs587776771
gopubmedrs587776771
geneviewrs587776771
scholarrs587776771
googlers587776771
pharmgkbrs587776771
gwascentralrs587776771
openSNPrs587776771
23andMers587776771
23andMe allrs587776771
SNP Nexus

SNPshotrs587776771
SNPdbers587776771
MSV3drs587776771
GWAS Ctlgrs587776771
Max Magnitude0
ClinVar
Risk rs587776771(GT,T;GT,T)
Alt rs587776771(GT,T;GT,T)
Reference rs587776771(CT;CT)
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,