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rs1064795112

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome2
Position227688227
GeneSLC19A3
is asnp
is mentioned by
dbSNPrs1064795112
dbSNP (old)rs1064795112
ClinGenrs1064795112
ebirs1064795112
HLIrs1064795112
Exacrs1064795112
Gnomadrs1064795112
Varsomers1064795112
Maprs1064795112
PheGenIrs1064795112
Biobankrs1064795112
1000 genomesrs1064795112
hgdprs1064795112
ensemblrs1064795112
gopubmedrs1064795112
geneviewrs1064795112
scholarrs1064795112
googlers1064795112
pharmgkbrs1064795112
gwascentralrs1064795112
openSNPrs1064795112
23andMers1064795112
23andMe allrs1064795112
SNPshotrs1064795112
SNPdbers1064795112
MSV3drs1064795112
GWAS Ctlgrs1064795112
Max Magnitude0
ClinVar
Risk rs1064795112(G;G)
Alt rs1064795112(G;G)
Reference Rs1064795112(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SLC19A3
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.228552943T>C
CLNSRC
CLNACC RCV000482702.1,