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rs121913033

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913033(A;A)
Make rs121913033(A;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position107779689
GeneSLC26A3
is asnp
is mentioned by
dbSNPrs121913033
ebirs121913033
HLIrs121913033
Exacrs121913033
Varsomers121913033
Maprs121913033
PheGenIrs121913033
hapmaprs121913033
1000 genomesrs121913033
hgdprs121913033
ensemblrs121913033
gopubmedrs121913033
geneviewrs121913033
scholarrs121913033
googlers121913033
pharmgkbrs121913033
gwascentralrs121913033
openSNPrs121913033
23andMers121913033
23andMe allrs121913033
SNP Nexus

SNPshotrs121913033
SNPdbers121913033
MSV3drs121913033
GWAS Ctlgrs121913033
Max Magnitude0
OMIM126650
Desc
Variant0008
Relatedalso
ClinVar
Risk rs121913033(A;A)
Alt rs121913033(A;A)
Reference rs121913033(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.107420134C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000018246.27,