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rs121918673

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121918673(C;G)
Make rs121918673(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position37701122
GeneHNF1B
is asnp
is mentioned by
dbSNPrs121918673
ebirs121918673
HLIrs121918673
Exacrs121918673
Varsomers121918673
Maprs121918673
PheGenIrs121918673
hapmaprs121918673
1000 genomesrs121918673
hgdprs121918673
ensemblrs121918673
gopubmedrs121918673
geneviewrs121918673
scholarrs121918673
googlers121918673
pharmgkbrs121918673
gwascentralrs121918673
openSNPrs121918673
23andMers121918673
23andMe allrs121918673
SNP Nexus

SNPshotrs121918673
SNPdbers121918673
MSV3drs121918673
GWAS Ctlgrs121918673
Max Magnitude0
OMIM189907
Desc
Variant0007
Relatedalso
ClinVar
Risk rs121918673(G;G)
Alt rs121918673(G;G)
Reference rs121918673(C;C)
Significance Pathogenic
Disease Diabetes mellitus type 2
Variation info
Gene HNF1B
CLNDBN Diabetes mellitus type 2
Reversed 1
HGVS NC_000017.10:g.36061127G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000013476.22,