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rs1057521967

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057521967(C;T)
Make rs1057521967(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position42929954
GeneSLC2A1
is asnp
is mentioned by
dbSNPrs1057521967
dbSNP (old)rs1057521967
ClinGenrs1057521967
ebirs1057521967
HLIrs1057521967
Exacrs1057521967
Gnomadrs1057521967
Varsomers1057521967
Maprs1057521967
PheGenIrs1057521967
Biobankrs1057521967
1000 genomesrs1057521967
hgdprs1057521967
ensemblrs1057521967
gopubmedrs1057521967
geneviewrs1057521967
scholarrs1057521967
googlers1057521967
pharmgkbrs1057521967
gwascentralrs1057521967
openSNPrs1057521967
23andMers1057521967
23andMe allrs1057521967
SNPshotrs1057521967
SNPdbers1057521967
MSV3drs1057521967
GWAS Ctlgrs1057521967
Max Magnitude0
ClinVar
Risk rs1057521967(T;T)
Alt rs1057521967(T;T)
Reference Rs1057521967(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SLC2A1
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.43395625G>A
CLNSRC
CLNACC RCV000429681.1,