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rs139722450

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs139722450(C;G)
Make rs139722450(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position42927627
GeneSLC2A1
is asnp
is mentioned by
dbSNPrs139722450
dbSNP (old)rs139722450
ClinGenrs139722450
ebirs139722450
HLIrs139722450
Exacrs139722450
Gnomadrs139722450
Varsomers139722450
LitVarrs139722450
Maprs139722450
PheGenIrs139722450
Biobankrs139722450
1000 genomesrs139722450
hgdprs139722450
ensemblrs139722450
gopubmedrs139722450
geneviewrs139722450
scholarrs139722450
googlers139722450
pharmgkbrs139722450
gwascentralrs139722450
openSNPrs139722450
23andMers139722450
23andMe allrs139722450
SNPshotrs139722450
SNPdbers139722450
MSV3drs139722450
GWAS Ctlgrs139722450
Max Magnitude0
ClinVar
Risk rs139722450(A;A) rs139722450(G;G)
Alt rs139722450(A;A) rs139722450(G;G)
Reference Rs139722450(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SLC2A1
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.43393298C>A
CLNSRC
CLNACC RCV000413602.1,