Have questions? Visit https://www.reddit.com/r/SNPedia

rs386833444

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs386833444(A;A)
Make rs386833444(A;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position107783296
GeneSLC26A3
is asnp
is mentioned by
dbSNPrs386833444
ebirs386833444
HLIrs386833444
Exacrs386833444
Varsomers386833444
Maprs386833444
PheGenIrs386833444
hapmaprs386833444
1000 genomesrs386833444
hgdprs386833444
ensemblrs386833444
gopubmedrs386833444
geneviewrs386833444
scholarrs386833444
googlers386833444
pharmgkbrs386833444
gwascentralrs386833444
openSNPrs386833444
23andMers386833444
23andMe allrs386833444
SNP Nexus

SNPshotrs386833444
SNPdbers386833444
MSV3drs386833444
GWAS Ctlgrs386833444
Max Magnitude0
ClinVar
Risk rs386833444(A,C;A,C)
Alt rs386833444(A,C;A,C)
Reference rs386833444(G;G)
Significance Probable-Pathogenic
Disease Congenital secretory diarrhea
Variation info
Gene SLC26A3
CLNDBN Congenital secretory diarrhea, chloride type
Reversed 1
HGVS NC_000007.13:g.107423741C>T
CLNSRC ClinVar
CLNACC RCV000049371.1,


[PMID 21394828] Update on SLC26A3 mutations in congenital chloride diarrhea.