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rs121913031

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs121913031(-;-)
Make rs121913031(-;ATC)
Make rs121913031(ATC;ATC)
ReferenceGRCh38 38.1/141
Chromosome7
Position107772090
GeneSLC26A3
is asnp
is mentioned by
dbSNPrs121913031
ebirs121913031
HLIrs121913031
Exacrs121913031
Varsomers121913031
Maprs121913031
PheGenIrs121913031
hapmaprs121913031
1000 genomesrs121913031
hgdprs121913031
ensemblrs121913031
gopubmedrs121913031
geneviewrs121913031
scholarrs121913031
googlers121913031
pharmgkbrs121913031
gwascentralrs121913031
openSNPrs121913031
23andMers121913031
23andMe allrs121913031
SNP Nexus

SNPshotrs121913031
SNPdbers121913031
MSV3drs121913031
GWAS Ctlgrs121913031
Max Magnitude0
OMIM126650
Desc
Variant0005
Relatedalso
ClinVar
Risk rs121913031(TCA;TCA)
Alt rs121913031(TCA;TCA)
Reference rs121913031(;)
Significance Other
Disease Congenital secretory diarrhea
Variation info
Gene SLC26A3
CLNDBN Congenital secretory diarrhea, chloride type
Reversed 1
HGVS NC_000007.13:g.107412535_107412537dupTGA
CLNSRC OMIM Allelic Variant
CLNACC RCV000049397.4,