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rs137853238

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137853238(A;A)
Make rs137853238(A;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position120994265
GeneHNF1A
is asnp
is mentioned by
dbSNPrs137853238
ebirs137853238
HLIrs137853238
Exacrs137853238
Varsomers137853238
Maprs137853238
PheGenIrs137853238
hapmaprs137853238
1000 genomesrs137853238
hgdprs137853238
ensemblrs137853238
gopubmedrs137853238
geneviewrs137853238
scholarrs137853238
googlers137853238
pharmgkbrs137853238
gwascentralrs137853238
openSNPrs137853238
23andMers137853238
23andMe allrs137853238
SNP Nexus

SNPshotrs137853238
SNPdbers137853238
MSV3drs137853238
GWAS Ctlgrs137853238
Max Magnitude0
OMIM142410
Desc
Variant0005
Relatedalso
ClinVar
Risk rs137853238(A;A)
Alt rs137853238(A;A)
Reference rs137853238(G;G)
Significance Pathogenic
Disease Diabetes mellitus
Variation info
Gene HNF1A
CLNDBN Diabetes mellitus, insulin-dependent, 20
Reversed 0
HGVS NC_000012.11:g.121432068G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000016068.23,