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rs121908404

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121908404(A;T)
Make rs121908404(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position38264893
GeneSPINT2
is asnp
is mentioned by
dbSNPrs121908404
ebirs121908404
HLIrs121908404
Exacrs121908404
Varsomers121908404
Maprs121908404
PheGenIrs121908404
hapmaprs121908404
1000 genomesrs121908404
hgdprs121908404
ensemblrs121908404
gopubmedrs121908404
geneviewrs121908404
scholarrs121908404
googlers121908404
pharmgkbrs121908404
gwascentralrs121908404
openSNPrs121908404
23andMers121908404
23andMe allrs121908404
SNP Nexus

SNPshotrs121908404
SNPdbers121908404
MSV3drs121908404
GWAS Ctlgrs121908404
Max Magnitude0
OMIM605124
Desc
Variant0005
Relatedalso
ClinVar
Risk rs121908404(T;T)
Alt rs121908404(T;T)
Reference rs121908404(A;A)
Significance Pathogenic
Disease Diarrhea 3
Variation info
Gene SPINT2
CLNDBN Diarrhea 3, secretory sodium, congenital, syndromic
Reversed 0
HGVS NC_000019.9:g.38755533A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000005518.3,