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rs794726933

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794726933(A;C)
Make rs794726933(C;C)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position74421990
GeneLOC105373252, SLC16A2
is asnp
is mentioned by
dbSNPrs794726933
ebirs794726933
HLIrs794726933
Exacrs794726933
Varsomers794726933
Maprs794726933
PheGenIrs794726933
hapmaprs794726933
1000 genomesrs794726933
hgdprs794726933
ensemblrs794726933
gopubmedrs794726933
geneviewrs794726933
scholarrs794726933
googlers794726933
pharmgkbrs794726933
gwascentralrs794726933
openSNPrs794726933
23andMers794726933
23andMe allrs794726933
SNP Nexus

SNPshotrs794726933
SNPdbers794726933
MSV3drs794726933
GWAS Ctlgrs794726933
Max Magnitude0
ClinVar
Risk rs794726933(C;C)
Alt rs794726933(C;C)
Reference rs794726933(A;A)
Significance Probable-Pathogenic
Disease Allan-Herndon-Dudley syndrome
Variation info
Gene SLC16A2
CLNDBN Allan-Herndon-Dudley syndrome
Reversed 0
HGVS NC_000023.10:g.73641825A>C
CLNSRC
CLNACC RCV000173415.1,