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rs796053272

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796053272(A;G)
Make rs796053272(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position42943323
GeneSLC2A1
is asnp
is mentioned by
dbSNPrs796053272
ebirs796053272
HLIrs796053272
Exacrs796053272
Varsomers796053272
Maprs796053272
PheGenIrs796053272
hapmaprs796053272
1000 genomesrs796053272
hgdprs796053272
ensemblrs796053272
gopubmedrs796053272
geneviewrs796053272
scholarrs796053272
googlers796053272
pharmgkbrs796053272
gwascentralrs796053272
openSNPrs796053272
23andMers796053272
23andMe allrs796053272
SNP Nexus

SNPshotrs796053272
SNPdbers796053272
MSV3drs796053272
GWAS Ctlgrs796053272
Max Magnitude0
ClinVar
Risk rs796053272(G;G)
Alt rs796053272(G;G)
Reference rs796053272(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene SLC2A1
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.43408994T>C
CLNSRC
CLNACC RCV000189392.1,