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rs1057521066

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057521066(C;T)
Make rs1057521066(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position42929616
GeneSLC2A1
is asnp
is mentioned by
dbSNPrs1057521066
dbSNP (classic)rs1057521066
ClinGenrs1057521066
ebirs1057521066
HLIrs1057521066
Exacrs1057521066
Gnomadrs1057521066
Varsomers1057521066
LitVarrs1057521066
Maprs1057521066
PheGenIrs1057521066
Biobankrs1057521066
1000 genomesrs1057521066
hgdprs1057521066
ensemblrs1057521066
geneviewrs1057521066
scholarrs1057521066
googlers1057521066
pharmgkbrs1057521066
gwascentralrs1057521066
openSNPrs1057521066
23andMers1057521066
23andMe allrs1057521066
SNPshotrs1057521066
SNPdbers1057521066
MSV3drs1057521066
GWAS Ctlgrs1057521066
Max Magnitude0
ClinVar
Risk rs1057521066(T;T)
Alt rs1057521066(T;T)
Reference Rs1057521066(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SLC2A1
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.43395287G>A
CLNSRC
CLNACC RCV000432773.1,