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rs386833465

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs386833465(-;-)
Make rs386833465(-;A)
ReferenceGRCh38 38.1/141
Chromosome7
Position107776520
GeneSLC26A3
is asnp
is mentioned by
dbSNPrs386833465
ebirs386833465
HLIrs386833465
Exacrs386833465
Varsomers386833465
Maprs386833465
PheGenIrs386833465
hapmaprs386833465
1000 genomesrs386833465
hgdprs386833465
ensemblrs386833465
gopubmedrs386833465
geneviewrs386833465
scholarrs386833465
googlers386833465
pharmgkbrs386833465
gwascentralrs386833465
openSNPrs386833465
23andMers386833465
23andMe allrs386833465
SNP Nexus

SNPshotrs386833465
SNPdbers386833465
MSV3drs386833465
GWAS Ctlgrs386833465
Max Magnitude0
ClinVar
Risk rs386833465(;)
Alt rs386833465(;)
Reference rs386833465(A;A)
Significance Probable-Pathogenic
Disease Congenital secretory diarrhea
Variation info
Gene SLC26A3
CLNDBN Congenital secretory diarrhea, chloride type
Reversed 1
HGVS NC_000007.13:g.107416965delT
CLNSRC ClinVar
CLNACC RCV000049392.1,


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