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

rs869312806

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869312806(C;T)
Make rs869312806(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position484520
GeneSLC9A3
is asnp
is mentioned by
dbSNPrs869312806
dbSNP (classic)rs869312806
ClinGenrs869312806
ebirs869312806
HLIrs869312806
Exacrs869312806
Gnomadrs869312806
Varsomers869312806
LitVarrs869312806
Maprs869312806
PheGenIrs869312806
Biobankrs869312806
1000 genomesrs869312806
hgdprs869312806
ensemblrs869312806
geneviewrs869312806
scholarrs869312806
googlers869312806
pharmgkbrs869312806
gwascentralrs869312806
openSNPrs869312806
23andMers869312806
SNPshotrs869312806
SNPdbers869312806
MSV3drs869312806
GWAS Ctlgrs869312806
Max Magnitude0
ClinVar
Risk rs869312806(T;T)
Alt rs869312806(T;T)
Reference Rs869312806(C;C)
Significance Pathogenic
Disease Diarrhea 8
Variation info
Gene SLC9A3
CLNDBN Diarrhea 8, secretory sodium, congenital
Reversed 1
HGVS NC_000005.9:g.484635G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000210219.2,