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rs386833457

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs386833457(G;G)
Make rs386833457(G;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position107778202
GeneSLC26A3
is asnp
is mentioned by
dbSNPrs386833457
ebirs386833457
HLIrs386833457
Exacrs386833457
Varsomers386833457
Maprs386833457
PheGenIrs386833457
hapmaprs386833457
1000 genomesrs386833457
hgdprs386833457
ensemblrs386833457
gopubmedrs386833457
geneviewrs386833457
scholarrs386833457
googlers386833457
pharmgkbrs386833457
gwascentralrs386833457
openSNPrs386833457
23andMers386833457
23andMe allrs386833457
SNP Nexus

SNPshotrs386833457
SNPdbers386833457
MSV3drs386833457
GWAS Ctlgrs386833457
Max Magnitude0
ClinVar
Risk rs386833457(G;G)
Alt rs386833457(G;G)
Reference rs386833457(T;T)
Significance Probable-Pathogenic
Disease Congenital secretory diarrhea
Variation info
Gene SLC26A3
CLNDBN Congenital secretory diarrhea, chloride type
Reversed 1
HGVS NC_000007.13:g.107418647A>C
CLNSRC ClinVar
CLNACC RCV000049384.1,


[PMID 9718329OA-icon.png] Genetic background of congenital chloride diarrhea in high-incidence populations: Finland, Poland, and Saudi Arabia and Kuwait.