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rs796053254

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796053254(A;A)
Make rs796053254(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position42929210
GeneSLC2A1
is asnp
is mentioned by
dbSNPrs796053254
ebirs796053254
HLIrs796053254
Exacrs796053254
Varsomers796053254
Maprs796053254
PheGenIrs796053254
hapmaprs796053254
1000 genomesrs796053254
hgdprs796053254
ensemblrs796053254
gopubmedrs796053254
geneviewrs796053254
scholarrs796053254
googlers796053254
pharmgkbrs796053254
gwascentralrs796053254
openSNPrs796053254
23andMers796053254
23andMe allrs796053254
SNP Nexus

SNPshotrs796053254
SNPdbers796053254
MSV3drs796053254
GWAS Ctlgrs796053254
Max Magnitude0
ClinVar
Risk rs796053254(A;A)
Alt rs796053254(A;A)
Reference rs796053254(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SLC2A1
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.43394881C>T
CLNSRC
CLNACC RCV000189367.2,