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rs1085307782

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome11
Position20638481
GeneSLC6A5
is asnp
is mentioned by
dbSNPrs1085307782
dbSNP (classic)rs1085307782
ClinGenrs1085307782
ebirs1085307782
HLIrs1085307782
Exacrs1085307782
Gnomadrs1085307782
Varsomers1085307782
LitVarrs1085307782
Maprs1085307782
PheGenIrs1085307782
Biobankrs1085307782
1000 genomesrs1085307782
hgdprs1085307782
ensemblrs1085307782
geneviewrs1085307782
scholarrs1085307782
googlers1085307782
pharmgkbrs1085307782
gwascentralrs1085307782
openSNPrs1085307782
23andMers1085307782
23andMe allrs1085307782
SNPshotrs1085307782
SNPdbers1085307782
MSV3drs1085307782
GWAS Ctlgrs1085307782
Max Magnitude0
ClinVar
Risk rs1085307782(C;C)
Alt rs1085307782(C;C)
Reference Rs1085307782(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SLC6A5
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.20660027T>C
CLNSRC
CLNACC RCV000489153.1,