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rs796053265

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796053265(-;-)
Make rs796053265(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position42931209
GeneSLC2A1
is asnp
is mentioned by
dbSNPrs796053265
ebirs796053265
HLIrs796053265
Exacrs796053265
Varsomers796053265
Maprs796053265
PheGenIrs796053265
hapmaprs796053265
1000 genomesrs796053265
hgdprs796053265
ensemblrs796053265
gopubmedrs796053265
geneviewrs796053265
scholarrs796053265
googlers796053265
pharmgkbrs796053265
gwascentralrs796053265
openSNPrs796053265
23andMers796053265
23andMe allrs796053265
SNP Nexus

SNPshotrs796053265
SNPdbers796053265
MSV3drs796053265
GWAS Ctlgrs796053265
Max Magnitude0
ClinVar
Risk rs796053265(;)
Alt rs796053265(;)
Reference rs796053265(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SLC2A1
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.43396880delG
CLNSRC
CLNACC RCV000189384.1,