Have questions? Visit https://www.reddit.com/r/SNPedia

rs121908403

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121908403(A;G)
Make rs121908403(G;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position38290215
GeneSPINT2
is asnp
is mentioned by
dbSNPrs121908403
ebirs121908403
HLIrs121908403
Exacrs121908403
Varsomers121908403
Maprs121908403
PheGenIrs121908403
hapmaprs121908403
1000 genomesrs121908403
hgdprs121908403
ensemblrs121908403
gopubmedrs121908403
geneviewrs121908403
scholarrs121908403
googlers121908403
pharmgkbrs121908403
gwascentralrs121908403
openSNPrs121908403
23andMers121908403
23andMe allrs121908403
SNP Nexus

SNPshotrs121908403
SNPdbers121908403
MSV3drs121908403
GWAS Ctlgrs121908403
Max Magnitude0
OMIM605124
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121908403(G;G)
Alt rs121908403(G;G)
Reference rs121908403(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.38780855A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000005515.3,