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rs1085308011

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
ChromosomeX
Position153694137
GeneSLC6A8
is asnp
is mentioned by
dbSNPrs1085308011
dbSNP (classic)rs1085308011
ClinGenrs1085308011
ebirs1085308011
HLIrs1085308011
Exacrs1085308011
Gnomadrs1085308011
Varsomers1085308011
LitVarrs1085308011
Maprs1085308011
PheGenIrs1085308011
Biobankrs1085308011
1000 genomesrs1085308011
hgdprs1085308011
ensemblrs1085308011
geneviewrs1085308011
scholarrs1085308011
googlers1085308011
pharmgkbrs1085308011
gwascentralrs1085308011
openSNPrs1085308011
23andMers1085308011
SNPshotrs1085308011
SNPdbers1085308011
MSV3drs1085308011
GWAS Ctlgrs1085308011
Max Magnitude0
ClinVar
Risk rs1085308011(A;A)
Alt rs1085308011(A;A)
Reference Rs1085308011(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SLC6A8
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.152959592G>A
CLNSRC
CLNACC RCV000490037.1,