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rs121918102

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121918102(G;T)
Make rs121918102(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position2159911
GeneINS, INS-IGF2
is asnp
is mentioned by
dbSNPrs121918102
ebirs121918102
HLIrs121918102
Exacrs121918102
Varsomers121918102
Maprs121918102
PheGenIrs121918102
hapmaprs121918102
1000 genomesrs121918102
hgdprs121918102
ensemblrs121918102
gopubmedrs121918102
geneviewrs121918102
scholarrs121918102
googlers121918102
pharmgkbrs121918102
gwascentralrs121918102
openSNPrs121918102
23andMers121918102
23andMe allrs121918102
SNP Nexus

SNPshotrs121918102
SNPdbers121918102
MSV3drs121918102
GWAS Ctlgrs121918102
Max Magnitude0
OMIM176730
Desc
Variant0005
Relatedalso
ClinVar
Risk rs121918102(T;T)
Alt rs121918102(T;T)
Reference rs121918102(G;G)
Significance Pathogenic
Disease Hyperproinsulinemia
Variation info
Gene INS IGF2 INS-IGF2
CLNDBN Hyperproinsulinemia
Reversed 1
HGVS NC_000011.9:g.2181141C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000014311.27,