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rs1057521632

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057521632(C;T)
Make rs1057521632(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position42927735
GeneSLC2A1
is asnp
is mentioned by
dbSNPrs1057521632
dbSNP (old)rs1057521632
ClinGenrs1057521632
ebirs1057521632
HLIrs1057521632
Exacrs1057521632
Gnomadrs1057521632
Varsomers1057521632
Maprs1057521632
PheGenIrs1057521632
Biobankrs1057521632
1000 genomesrs1057521632
hgdprs1057521632
ensemblrs1057521632
gopubmedrs1057521632
geneviewrs1057521632
scholarrs1057521632
googlers1057521632
pharmgkbrs1057521632
gwascentralrs1057521632
openSNPrs1057521632
23andMers1057521632
23andMe allrs1057521632
SNPshotrs1057521632
SNPdbers1057521632
MSV3drs1057521632
GWAS Ctlgrs1057521632
Max Magnitude0
ClinVar
Risk rs1057521632(T;T)
Alt rs1057521632(T;T)
Reference Rs1057521632(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SLC2A1
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.43393406G>A
CLNSRC
CLNACC RCV000442546.1,