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rs1064794334

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome6
Position73610398
GeneSLC17A5
is asnp
is mentioned by
dbSNPrs1064794334
dbSNP (old)rs1064794334
ClinGenrs1064794334
ebirs1064794334
HLIrs1064794334
Exacrs1064794334
Gnomadrs1064794334
Varsomers1064794334
Maprs1064794334
PheGenIrs1064794334
Biobankrs1064794334
1000 genomesrs1064794334
hgdprs1064794334
ensemblrs1064794334
gopubmedrs1064794334
geneviewrs1064794334
scholarrs1064794334
googlers1064794334
pharmgkbrs1064794334
gwascentralrs1064794334
openSNPrs1064794334
23andMers1064794334
23andMe allrs1064794334
SNPshotrs1064794334
SNPdbers1064794334
MSV3drs1064794334
GWAS Ctlgrs1064794334
Max Magnitude0
ClinVar
Risk rs1064794334(C;C)
Alt rs1064794334(C;C)
Reference Rs1064794334(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene SLC17A5
CLNDBN not provided
Reversed 1
HGVS NC_000006.11:g.74320121A>G
CLNSRC
CLNACC RCV000485108.1,