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rs796053249

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796053249(A;T)
Make rs796053249(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position42929753
GeneSLC2A1
is asnp
is mentioned by
dbSNPrs796053249
ebirs796053249
HLIrs796053249
Exacrs796053249
Varsomers796053249
Maprs796053249
PheGenIrs796053249
hapmaprs796053249
1000 genomesrs796053249
hgdprs796053249
ensemblrs796053249
gopubmedrs796053249
geneviewrs796053249
scholarrs796053249
googlers796053249
pharmgkbrs796053249
gwascentralrs796053249
openSNPrs796053249
23andMers796053249
23andMe allrs796053249
SNP Nexus

SNPshotrs796053249
SNPdbers796053249
MSV3drs796053249
GWAS Ctlgrs796053249
Max Magnitude0
ClinVar
Risk rs796053249(T;T)
Alt rs796053249(T;T)
Reference rs796053249(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SLC2A1
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.43395424T>A
CLNSRC
CLNACC RCV000189357.1,