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

rs121913030

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121913030(A;T)
Make rs121913030(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position107791841
GeneSLC26A3
is asnp
is mentioned by
dbSNPrs121913030
ebirs121913030
HLIrs121913030
Exacrs121913030
Varsomers121913030
Maprs121913030
PheGenIrs121913030
hapmaprs121913030
1000 genomesrs121913030
hgdprs121913030
ensemblrs121913030
gopubmedrs121913030
geneviewrs121913030
scholarrs121913030
googlers121913030
pharmgkbrs121913030
gwascentralrs121913030
openSNPrs121913030
23andMers121913030
23andMe allrs121913030
SNP Nexus

SNPshotrs121913030
SNPdbers121913030
MSV3drs121913030
GWAS Ctlgrs121913030
Max Magnitude0
OMIM126650
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121913030(T;T)
Alt rs121913030(T;T)
Reference rs121913030(A;A)
Significance Pathogenic
Disease Congenital secretory diarrhea
Variation info
Gene SLC26A3
CLNDBN Congenital secretory diarrhea, chloride type
Reversed 1
HGVS NC_000007.13:g.107432286T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000018240.23,