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rs796053253

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796053253(C;T)
Make rs796053253(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position42929211
GeneSLC2A1
is asnp
is mentioned by
dbSNPrs796053253
ebirs796053253
HLIrs796053253
Exacrs796053253
Varsomers796053253
Maprs796053253
PheGenIrs796053253
hapmaprs796053253
1000 genomesrs796053253
hgdprs796053253
ensemblrs796053253
gopubmedrs796053253
geneviewrs796053253
scholarrs796053253
googlers796053253
pharmgkbrs796053253
gwascentralrs796053253
openSNPrs796053253
23andMers796053253
23andMe allrs796053253
SNP Nexus

SNPshotrs796053253
SNPdbers796053253
MSV3drs796053253
GWAS Ctlgrs796053253
Max Magnitude0
ClinVar
Risk rs796053253(T;T)
Alt rs796053253(T;T)
Reference rs796053253(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SLC2A1
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.43394882G>A
CLNSRC
CLNACC RCV000189366.2,