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rs794726932

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794726932(A;A)
Make rs794726932(A;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position74421963
GeneLOC105373252, SLC16A2
is asnp
is mentioned by
dbSNPrs794726932
ebirs794726932
HLIrs794726932
Exacrs794726932
Varsomers794726932
Maprs794726932
PheGenIrs794726932
hapmaprs794726932
1000 genomesrs794726932
hgdprs794726932
ensemblrs794726932
gopubmedrs794726932
geneviewrs794726932
scholarrs794726932
googlers794726932
pharmgkbrs794726932
gwascentralrs794726932
openSNPrs794726932
23andMers794726932
23andMe allrs794726932
SNP Nexus

SNPshotrs794726932
SNPdbers794726932
MSV3drs794726932
GWAS Ctlgrs794726932
Max Magnitude0
ClinVar
Risk rs794726932(A;A)
Alt rs794726932(A;A)
Reference rs794726932(G;G)
Significance Pathogenic
Disease Allan-Herndon-Dudley syndrome
Variation info
Gene SLC16A2
CLNDBN Allan-Herndon-Dudley syndrome
Reversed 0
HGVS NC_000023.10:g.73641798G>A
CLNSRC
CLNACC RCV000173414.1,