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rs121913032

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913032(G;T)
Make rs121913032(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position107791059
GeneSLC26A3
is asnp
is mentioned by
dbSNPrs121913032
ebirs121913032
HLIrs121913032
Exacrs121913032
Varsomers121913032
Maprs121913032
PheGenIrs121913032
hapmaprs121913032
1000 genomesrs121913032
hgdprs121913032
ensemblrs121913032
gopubmedrs121913032
geneviewrs121913032
scholarrs121913032
googlers121913032
pharmgkbrs121913032
gwascentralrs121913032
openSNPrs121913032
23andMers121913032
23andMe allrs121913032
SNP Nexus

SNPshotrs121913032
SNPdbers121913032
MSV3drs121913032
GWAS Ctlgrs121913032
Max Magnitude0
OMIM126650
Desc
Variant0006
Relatedalso
ClinVar
Risk rs121913032(T;T)
Alt rs121913032(T;T)
Reference rs121913032(G;G)
Significance Pathogenic
Disease Congenital secretory diarrhea
Variation info
Gene SLC26A3
CLNDBN Congenital secretory diarrhea, chloride type
Reversed 1
HGVS NC_000007.13:g.107431504C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000018244.24,