Have questions? Visit https://www.reddit.com/r/SNPedia

rs1085307963

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome2
Position227688252
GeneSLC19A3
is asnp
is mentioned by
dbSNPrs1085307963
dbSNP (old)rs1085307963
ClinGenrs1085307963
ebirs1085307963
HLIrs1085307963
Exacrs1085307963
Gnomadrs1085307963
Varsomers1085307963
Maprs1085307963
PheGenIrs1085307963
Biobankrs1085307963
1000 genomesrs1085307963
hgdprs1085307963
ensemblrs1085307963
gopubmedrs1085307963
geneviewrs1085307963
scholarrs1085307963
googlers1085307963
pharmgkbrs1085307963
gwascentralrs1085307963
openSNPrs1085307963
23andMers1085307963
23andMe allrs1085307963
SNPshotrs1085307963
SNPdbers1085307963
MSV3drs1085307963
GWAS Ctlgrs1085307963
Max Magnitude0
ClinVar
Risk rs1085307963(C;C)
Alt rs1085307963(C;C)
Reference Rs1085307963(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SLC19A3
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.228552968T>G
CLNSRC
CLNACC RCV000489741.1,