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rs121918101

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121918101(C;G)
Make rs121918101(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position2160872
GeneINS, INS-IGF2
is asnp
is mentioned by
dbSNPrs121918101
ebirs121918101
HLIrs121918101
Exacrs121918101
Varsomers121918101
Maprs121918101
PheGenIrs121918101
hapmaprs121918101
1000 genomesrs121918101
hgdprs121918101
ensemblrs121918101
gopubmedrs121918101
geneviewrs121918101
scholarrs121918101
googlers121918101
pharmgkbrs121918101
gwascentralrs121918101
openSNPrs121918101
23andMers121918101
23andMe allrs121918101
SNP Nexus

SNPshotrs121918101
SNPdbers121918101
MSV3drs121918101
GWAS Ctlgrs121918101
Max Magnitude0
OMIM176730
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121918101(G;G)
Alt rs121918101(G;G)
Reference rs121918101(C;C)
Significance Pathogenic
Disease Hyperproinsulinemia
Variation info
Gene INS INS-IGF2
CLNDBN Hyperproinsulinemia
Reversed 1
HGVS NC_000011.9:g.2182102G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000014308.26,