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rs796053250

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796053250(C;T)
Make rs796053250(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position42929715
GeneSLC2A1
is asnp
is mentioned by
dbSNPrs796053250
ebirs796053250
HLIrs796053250
Exacrs796053250
Varsomers796053250
Maprs796053250
PheGenIrs796053250
hapmaprs796053250
1000 genomesrs796053250
hgdprs796053250
ensemblrs796053250
gopubmedrs796053250
geneviewrs796053250
scholarrs796053250
googlers796053250
pharmgkbrs796053250
gwascentralrs796053250
openSNPrs796053250
23andMers796053250
23andMe allrs796053250
SNP Nexus

SNPshotrs796053250
SNPdbers796053250
MSV3drs796053250
GWAS Ctlgrs796053250
Max Magnitude0
ClinVar
Risk rs796053250(T;T)
Alt rs796053250(T;T)
Reference rs796053250(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SLC2A1
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.43395386G>A
CLNSRC
CLNACC RCV000189358.1,