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rs121917838

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121917838(G;T)
Make rs121917838(T;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position69572766
GeneNEUROG3
is asnp
is mentioned by
dbSNPrs121917838
ebirs121917838
HLIrs121917838
Exacrs121917838
Varsomers121917838
Maprs121917838
PheGenIrs121917838
hapmaprs121917838
1000 genomesrs121917838
hgdprs121917838
ensemblrs121917838
gopubmedrs121917838
geneviewrs121917838
scholarrs121917838
googlers121917838
pharmgkbrs121917838
gwascentralrs121917838
openSNPrs121917838
23andMers121917838
23andMe allrs121917838
SNP Nexus

SNPshotrs121917838
SNPdbers121917838
MSV3drs121917838
GWAS Ctlgrs121917838
Max Magnitude0
ClinVar
Risk rs121917838(T;T)
Alt rs121917838(T;T)
Reference rs121917838(G;G)
Significance Pathogenic
Disease Diarrhea 4
Variation info
Gene NEUROG3
CLNDBN Diarrhea 4, malabsorptive, congenital
Reversed 1
HGVS NC_000010.10:g.71332522C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000005649.2,