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rs796053266

From SNPedia

Orientationminus
Geno Mag Summary
(GGCCATCTTT;GGCCATCTTT) 0 common in clinvar
Make rs796053266(C;C)
Make rs796053266(C;GGCCATCTTT)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position42931105
GeneSLC2A1
is asnp
is mentioned by
dbSNPrs796053266
ebirs796053266
HLIrs796053266
Exacrs796053266
Varsomers796053266
Maprs796053266
PheGenIrs796053266
hapmaprs796053266
1000 genomesrs796053266
hgdprs796053266
ensemblrs796053266
gopubmedrs796053266
geneviewrs796053266
scholarrs796053266
googlers796053266
pharmgkbrs796053266
gwascentralrs796053266
openSNPrs796053266
23andMers796053266
23andMe allrs796053266
SNP Nexus

SNPshotrs796053266
SNPdbers796053266
MSV3drs796053266
GWAS Ctlgrs796053266
Max Magnitude0
ClinVar
Risk rs796053266(C;C)
Alt rs796053266(C;C)
Reference rs796053266(GGCCATCTTT;GGCCATCTTT)
Significance Pathogenic
Disease not provided
Variation info
Gene SLC2A1
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.43396776_43396785delAAAGATGGCCinsG
CLNSRC
CLNACC RCV000189385.1,