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rs386833476

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs386833476(-;-)
Make rs386833476(-;AA)
Make rs386833476(AA;AA)
ReferenceGRCh38 38.1/141
Chromosome7
Position107793742
GeneSLC26A3
is asnp
is mentioned by
dbSNPrs386833476
ebirs386833476
HLIrs386833476
Exacrs386833476
Varsomers386833476
Maprs386833476
PheGenIrs386833476
hapmaprs386833476
1000 genomesrs386833476
hgdprs386833476
ensemblrs386833476
gopubmedrs386833476
geneviewrs386833476
scholarrs386833476
googlers386833476
pharmgkbrs386833476
gwascentralrs386833476
openSNPrs386833476
23andMers386833476
23andMe allrs386833476
SNP Nexus

SNPshotrs386833476
SNPdbers386833476
MSV3drs386833476
GWAS Ctlgrs386833476
Max Magnitude0
ClinVar
Risk rs386833476(AA;AA)
Alt rs386833476(AA;AA)
Reference rs386833476(;)
Significance Probable-Pathogenic
Disease Congenital secretory diarrhea
Variation info
Gene SLC26A3
CLNDBN Congenital secretory diarrhea, chloride type
Reversed 1
HGVS NC_000007.13:g.107434188_107434189dupTT
CLNSRC ClinVar
CLNACC RCV000049403.1,


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