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rs796053273

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796053273(A;A)
Make rs796053273(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position42943261
GeneSLC2A1
is asnp
is mentioned by
dbSNPrs796053273
ebirs796053273
HLIrs796053273
Exacrs796053273
Varsomers796053273
Maprs796053273
PheGenIrs796053273
hapmaprs796053273
1000 genomesrs796053273
hgdprs796053273
ensemblrs796053273
gopubmedrs796053273
geneviewrs796053273
scholarrs796053273
googlers796053273
pharmgkbrs796053273
gwascentralrs796053273
openSNPrs796053273
23andMers796053273
23andMe allrs796053273
SNP Nexus

SNPshotrs796053273
SNPdbers796053273
MSV3drs796053273
GWAS Ctlgrs796053273
Max Magnitude0
ClinVar
Risk rs796053273(A;A)
Alt rs796053273(A;A)
Reference rs796053273(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SLC2A1
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.43408932C>T
CLNSRC
CLNACC RCV000189393.1,