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rs796053267

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796053267(-;-)
Make rs796053267(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position42930013
GeneSLC2A1
is asnp
is mentioned by
dbSNPrs796053267
ebirs796053267
HLIrs796053267
Exacrs796053267
Varsomers796053267
Maprs796053267
PheGenIrs796053267
hapmaprs796053267
1000 genomesrs796053267
hgdprs796053267
ensemblrs796053267
gopubmedrs796053267
geneviewrs796053267
scholarrs796053267
googlers796053267
pharmgkbrs796053267
gwascentralrs796053267
openSNPrs796053267
23andMers796053267
23andMe allrs796053267
SNP Nexus

SNPshotrs796053267
SNPdbers796053267
MSV3drs796053267
GWAS Ctlgrs796053267
Max Magnitude0
ClinVar
Risk rs796053267(;)
Alt rs796053267(;)
Reference rs796053267(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene SLC2A1
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.43395684delA
CLNSRC
CLNACC RCV000189386.1,