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rs796053247

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796053247(C;T)
Make rs796053247(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position42929921
GeneSLC2A1
is asnp
is mentioned by
dbSNPrs796053247
ebirs796053247
HLIrs796053247
Exacrs796053247
Varsomers796053247
Maprs796053247
PheGenIrs796053247
hapmaprs796053247
1000 genomesrs796053247
hgdprs796053247
ensemblrs796053247
gopubmedrs796053247
geneviewrs796053247
scholarrs796053247
googlers796053247
pharmgkbrs796053247
gwascentralrs796053247
openSNPrs796053247
23andMers796053247
23andMe allrs796053247
SNP Nexus

SNPshotrs796053247
SNPdbers796053247
MSV3drs796053247
GWAS Ctlgrs796053247
Max Magnitude0
ClinVar
Risk rs796053247(T;T)
Alt rs796053247(T;T)
Reference rs796053247(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SLC2A1
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.43395592G>A
CLNSRC
CLNACC RCV000189354.2,