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rs796053270

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796053270(-;-)
Make rs796053270(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position42929027
GeneSLC2A1
is asnp
is mentioned by
dbSNPrs796053270
ebirs796053270
HLIrs796053270
Exacrs796053270
Varsomers796053270
Maprs796053270
PheGenIrs796053270
hapmaprs796053270
1000 genomesrs796053270
hgdprs796053270
ensemblrs796053270
gopubmedrs796053270
geneviewrs796053270
scholarrs796053270
googlers796053270
pharmgkbrs796053270
gwascentralrs796053270
openSNPrs796053270
23andMers796053270
23andMe allrs796053270
SNP Nexus

SNPshotrs796053270
SNPdbers796053270
MSV3drs796053270
GWAS Ctlgrs796053270
Max Magnitude0
ClinVar
Risk rs796053270(;)
Alt rs796053270(;)
Reference rs796053270(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SLC2A1
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.43394698delC
CLNSRC
CLNACC RCV000189390.1,