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rs753280877

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs753280877(A;A)
Make rs753280877(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position46725350
GeneSLC2A10
is asnp
is mentioned by
dbSNPrs753280877
ebirs753280877
HLIrs753280877
Exacrs753280877
Varsomers753280877
Maprs753280877
PheGenIrs753280877
hapmaprs753280877
1000 genomesrs753280877
hgdprs753280877
ensemblrs753280877
gopubmedrs753280877
geneviewrs753280877
scholarrs753280877
googlers753280877
pharmgkbrs753280877
gwascentralrs753280877
openSNPrs753280877
23andMers753280877
23andMe allrs753280877
SNP Nexus

SNPshotrs753280877
SNPdbers753280877
MSV3drs753280877
GWAS Ctlgrs753280877
Max Magnitude0
ClinVar
Risk rs753280877(A;A)
Alt rs753280877(A;A)
Reference rs753280877(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SLC2A10
CLNDBN not provided
Reversed 0
HGVS NC_000020.10:g.45353989G>A
CLNSRC
CLNACC RCV000199398.1,