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rs139858464

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs139858464(A;G)
Make rs139858464(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome20
Position46725452
GeneSLC2A10
is asnp
is mentioned by
dbSNPrs139858464
dbSNP (classic)rs139858464
ClinGenrs139858464
ebirs139858464
HLIrs139858464
Exacrs139858464
Gnomadrs139858464
Varsomers139858464
LitVarrs139858464
Maprs139858464
PheGenIrs139858464
Biobankrs139858464
1000 genomesrs139858464
hgdprs139858464
ensemblrs139858464
geneviewrs139858464
scholarrs139858464
googlers139858464
pharmgkbrs139858464
gwascentralrs139858464
openSNPrs139858464
23andMers139858464
SNPshotrs139858464
SNPdbers139858464
MSV3drs139858464
GWAS Ctlgrs139858464
Max Magnitude0
ClinVar
Risk rs139858464(G;G)
Alt rs139858464(G;G)
Reference Rs139858464(A;A)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene SLC2A10
CLNDBN not specified
Reversed 0
HGVS NC_000020.10:g.45354091A>G
CLNSRC
CLNACC RCV000200509.2,