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rs797045966

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs797045966(-;-)
Make rs797045966(-;A)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position74422011
GeneLOC105373252, SLC16A2
is asnp
is mentioned by
dbSNPrs797045966
dbSNP (old)rs797045966
ClinGenrs797045966
ebirs797045966
HLIrs797045966
Exacrs797045966
Varsomers797045966
Maprs797045966
PheGenIrs797045966
Biobankrs797045966
1000 genomesrs797045966
hgdprs797045966
ensemblrs797045966
gopubmedrs797045966
geneviewrs797045966
scholarrs797045966
googlers797045966
pharmgkbrs797045966
gwascentralrs797045966
openSNPrs797045966
23andMers797045966
23andMe allrs797045966
SNP Nexus

SNPshotrs797045966
SNPdbers797045966
MSV3drs797045966
GWAS Ctlgrs797045966
Max Magnitude0
ClinVar
Risk rs797045966(-;-)
Alt rs797045966(-;-)
Reference Rs797045966(A;A)
Significance Pathogenic
Disease Allan-Herndon-Dudley syndrome
Variation info
Gene SLC16A2
CLNDBN Allan-Herndon-Dudley syndrome
Reversed 0
HGVS NC_000023.10:g.73641846delA
CLNSRC
CLNACC RCV000193992.1,