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rs796053269

From SNPedia

Orientationminus
Geno Mag Summary
(GTG;GTG) 0 common in clinvar
Make rs796053269(-;-)
Make rs796053269(-;GTG)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position42929207
GeneSLC2A1
is asnp
is mentioned by
dbSNPrs796053269
ebirs796053269
HLIrs796053269
Exacrs796053269
Varsomers796053269
Maprs796053269
PheGenIrs796053269
hapmaprs796053269
1000 genomesrs796053269
hgdprs796053269
ensemblrs796053269
gopubmedrs796053269
geneviewrs796053269
scholarrs796053269
googlers796053269
pharmgkbrs796053269
gwascentralrs796053269
openSNPrs796053269
23andMers796053269
23andMe allrs796053269
SNP Nexus

SNPshotrs796053269
SNPdbers796053269
MSV3drs796053269
GWAS Ctlgrs796053269
Max Magnitude0
ClinVar
Risk rs796053269(;)
Alt rs796053269(;)
Reference rs796053269(GTG;GTG)
Significance Pathogenic
Disease not provided
Variation info
Gene SLC2A1
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.43394878_43394880delCAC
CLNSRC
CLNACC RCV000189389.1,