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rs796053264

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796053264(G;G)
Make rs796053264(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position42927611
GeneSLC2A1
is asnp
is mentioned by
dbSNPrs796053264
ebirs796053264
HLIrs796053264
Exacrs796053264
Varsomers796053264
Maprs796053264
PheGenIrs796053264
hapmaprs796053264
1000 genomesrs796053264
hgdprs796053264
ensemblrs796053264
gopubmedrs796053264
geneviewrs796053264
scholarrs796053264
googlers796053264
pharmgkbrs796053264
gwascentralrs796053264
openSNPrs796053264
23andMers796053264
23andMe allrs796053264
SNP Nexus

SNPshotrs796053264
SNPdbers796053264
MSV3drs796053264
GWAS Ctlgrs796053264
Max Magnitude0
ClinVar
Risk rs796053264(G;G)
Alt rs796053264(G;G)
Reference rs796053264(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene SLC2A1
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.43393282A>C
CLNSRC
CLNACC RCV000189379.1,