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rs776026092

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AGA;AGA) 0 common in clinvar
(I;I) 0 common genotype
Make rs776026092(-;-)
Make rs776026092(-;AGA)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position491931
GeneSLC9A3
is asnp
is mentioned by
dbSNPrs776026092
dbSNP (classic)rs776026092
ClinGenrs776026092
ebirs776026092
HLIrs776026092
Exacrs776026092
Gnomadrs776026092
Varsomers776026092
LitVarrs776026092
Maprs776026092
PheGenIrs776026092
Biobankrs776026092
1000 genomesrs776026092
hgdprs776026092
ensemblrs776026092
geneviewrs776026092
scholarrs776026092
googlers776026092
pharmgkbrs776026092
gwascentralrs776026092
openSNPrs776026092
23andMers776026092
SNPshotrs776026092
SNPdbers776026092
MSV3drs776026092
GWAS Ctlgrs776026092
Max Magnitude0
ClinVar
Risk rs776026092(-;-)
Alt rs776026092(-;-)
Reference Rs776026092(AGA;AGA)
Significance Pathogenic
Disease Diarrhea 8
Variation info
Gene SLC9A3
CLNDBN Diarrhea 8, secretory sodium, congenital
Reversed 0
HGVS NC_000005.9:g.492046_492048delAGA
CLNSRC OMIM Allelic Variant
CLNACC RCV000210210.2,