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rs1064795363

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome1
Position42929729
GeneSLC2A1
is asnp
is mentioned by
dbSNPrs1064795363
dbSNP (old)rs1064795363
ClinGenrs1064795363
ebirs1064795363
HLIrs1064795363
Exacrs1064795363
Gnomadrs1064795363
Varsomers1064795363
Maprs1064795363
PheGenIrs1064795363
Biobankrs1064795363
1000 genomesrs1064795363
hgdprs1064795363
ensemblrs1064795363
gopubmedrs1064795363
geneviewrs1064795363
scholarrs1064795363
googlers1064795363
pharmgkbrs1064795363
gwascentralrs1064795363
openSNPrs1064795363
23andMers1064795363
23andMe allrs1064795363
SNPshotrs1064795363
SNPdbers1064795363
MSV3drs1064795363
GWAS Ctlgrs1064795363
Max Magnitude0
ClinVar
Risk rs1064795363(G;G)
Alt rs1064795363(G;G)
Reference Rs1064795363(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SLC2A1
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.43395400A>C
CLNSRC
CLNACC RCV000482535.1,