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rs148800393

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs148800393(C;T)
Make rs148800393(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position42927667
GeneSLC2A1
is asnp
is mentioned by
dbSNPrs148800393
ebirs148800393
HLIrs148800393
Exacrs148800393
Varsomers148800393
Maprs148800393
PheGenIrs148800393
hapmaprs148800393
1000 genomesrs148800393
hgdprs148800393
ensemblrs148800393
gopubmedrs148800393
geneviewrs148800393
scholarrs148800393
googlers148800393
pharmgkbrs148800393
gwascentralrs148800393
openSNPrs148800393
23andMers148800393
23andMe allrs148800393
SNP Nexus

SNPshotrs148800393
SNPdbers148800393
MSV3drs148800393
GWAS Ctlgrs148800393
Max Magnitude0
ClinVar
Risk rs148800393(T;T)
Alt rs148800393(T;T)
Reference rs148800393(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SLC2A1
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.43393338C>T
CLNSRC
CLNACC RCV000189398.1,