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rs1064794836

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
ChromosomeX
Position153693175
GeneSLC6A8
is asnp
is mentioned by
dbSNPrs1064794836
dbSNP (old)rs1064794836
ClinGenrs1064794836
ebirs1064794836
HLIrs1064794836
Exacrs1064794836
Gnomadrs1064794836
Varsomers1064794836
LitVarrs1064794836
Maprs1064794836
PheGenIrs1064794836
Biobankrs1064794836
1000 genomesrs1064794836
hgdprs1064794836
ensemblrs1064794836
gopubmedrs1064794836
geneviewrs1064794836
scholarrs1064794836
googlers1064794836
pharmgkbrs1064794836
gwascentralrs1064794836
openSNPrs1064794836
23andMers1064794836
23andMe allrs1064794836
SNPshotrs1064794836
SNPdbers1064794836
MSV3drs1064794836
GWAS Ctlgrs1064794836
Max Magnitude0
ClinVar
Risk rs1064794836(C;C)
Alt rs1064794836(C;C)
Reference Rs1064794836(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SLC6A8
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.152958630G>C
CLNSRC
CLNACC RCV000483324.1,