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rs137853246

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;G) 2 associated with MODY3; maturity onset of diabetes in the young (type 3)
(G;G) 0 common in clinvar


Make rs137853246(C;C)
ReferenceGRCh38 38.1/141
Chromosome12
Position120999358
GeneHNF1A
is asnp
is mentioned by
dbSNPrs137853246
ebirs137853246
HLIrs137853246
Exacrs137853246
Varsomers137853246
Maprs137853246
PheGenIrs137853246
hapmaprs137853246
1000 genomesrs137853246
hgdprs137853246
ensemblrs137853246
gopubmedrs137853246
geneviewrs137853246
scholarrs137853246
googlers137853246
pharmgkbrs137853246
gwascentralrs137853246
openSNPrs137853246
23andMers137853246
23andMe allrs137853246
SNP Nexus

SNPshotrs137853246
SNPdbers137853246
MSV3drs137853246
GWAS Ctlgrs137853246
Max Magnitude2
OMIM142410
Desc
Variant0021
Relatedalso
ClinVar
Risk rs137853246(C;C)
Alt rs137853246(C;C)
Reference rs137853246(G;G)
Significance Pathogenic
Disease Maturity-onset diabetes of the young
Variation info
Gene HNF1A
CLNDBN Maturity-onset diabetes of the young, type 3
Reversed 0
HGVS NC_000012.11:g.121437161G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000016085.26,