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rs796053262

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796053262(G;G)
Make rs796053262(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position42927726
GeneSLC2A1
is asnp
is mentioned by
dbSNPrs796053262
ebirs796053262
HLIrs796053262
Exacrs796053262
Varsomers796053262
Maprs796053262
PheGenIrs796053262
hapmaprs796053262
1000 genomesrs796053262
hgdprs796053262
ensemblrs796053262
gopubmedrs796053262
geneviewrs796053262
scholarrs796053262
googlers796053262
pharmgkbrs796053262
gwascentralrs796053262
openSNPrs796053262
23andMers796053262
23andMe allrs796053262
SNP Nexus

SNPshotrs796053262
SNPdbers796053262
MSV3drs796053262
GWAS Ctlgrs796053262
Max Magnitude0
ClinVar
Risk rs796053262(G;G)
Alt rs796053262(G;G)
Reference rs796053262(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SLC2A1
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.43393397A>C
CLNSRC
CLNACC RCV000189377.1,