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rs796053255

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796053255(G;T)
Make rs796053255(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position42929024
GeneSLC2A1
is asnp
is mentioned by
dbSNPrs796053255
ebirs796053255
HLIrs796053255
Exacrs796053255
Varsomers796053255
Maprs796053255
PheGenIrs796053255
hapmaprs796053255
1000 genomesrs796053255
hgdprs796053255
ensemblrs796053255
gopubmedrs796053255
geneviewrs796053255
scholarrs796053255
googlers796053255
pharmgkbrs796053255
gwascentralrs796053255
openSNPrs796053255
23andMers796053255
23andMe allrs796053255
SNP Nexus

SNPshotrs796053255
SNPdbers796053255
MSV3drs796053255
GWAS Ctlgrs796053255
Max Magnitude0
ClinVar
Risk rs796053255(T;T)
Alt rs796053255(T;T)
Reference rs796053255(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SLC2A1
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.43394695C>A
CLNSRC
CLNACC RCV000189368.1,