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rs796053251

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796053251(A;G)
Make rs796053251(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position42929612
GeneSLC2A1
is asnp
is mentioned by
dbSNPrs796053251
ebirs796053251
HLIrs796053251
Exacrs796053251
Varsomers796053251
Maprs796053251
PheGenIrs796053251
hapmaprs796053251
1000 genomesrs796053251
hgdprs796053251
ensemblrs796053251
gopubmedrs796053251
geneviewrs796053251
scholarrs796053251
googlers796053251
pharmgkbrs796053251
gwascentralrs796053251
openSNPrs796053251
23andMers796053251
23andMe allrs796053251
SNP Nexus

SNPshotrs796053251
SNPdbers796053251
MSV3drs796053251
GWAS Ctlgrs796053251
Max Magnitude0
ClinVar
Risk rs796053251(G;G)
Alt rs796053251(G;G)
Reference rs796053251(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene SLC2A1
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.43395283T>C
CLNSRC
CLNACC RCV000189362.2,