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rs796053271

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796053271(-;-)
Make rs796053271(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position42929000
GeneSLC2A1
is asnp
is mentioned by
dbSNPrs796053271
ebirs796053271
HLIrs796053271
Exacrs796053271
Varsomers796053271
Maprs796053271
PheGenIrs796053271
hapmaprs796053271
1000 genomesrs796053271
hgdprs796053271
ensemblrs796053271
gopubmedrs796053271
geneviewrs796053271
scholarrs796053271
googlers796053271
pharmgkbrs796053271
gwascentralrs796053271
openSNPrs796053271
23andMers796053271
23andMe allrs796053271
SNP Nexus

SNPshotrs796053271
SNPdbers796053271
MSV3drs796053271
GWAS Ctlgrs796053271
Max Magnitude0
ClinVar
Risk rs796053271(;)
Alt rs796053271(;)
Reference rs796053271(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SLC2A1
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.43394671delG
CLNSRC
CLNACC RCV000189391.1,