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rs1057517822

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517822(A;A)
Make rs1057517822(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position42930724
GeneSLC2A1
is asnp
is mentioned by
dbSNPrs1057517822
dbSNP (old)rs1057517822
ClinGenrs1057517822
ebirs1057517822
HLIrs1057517822
Exacrs1057517822
Gnomadrs1057517822
Varsomers1057517822
Maprs1057517822
PheGenIrs1057517822
Biobankrs1057517822
1000 genomesrs1057517822
hgdprs1057517822
ensemblrs1057517822
gopubmedrs1057517822
geneviewrs1057517822
scholarrs1057517822
googlers1057517822
pharmgkbrs1057517822
gwascentralrs1057517822
openSNPrs1057517822
23andMers1057517822
23andMe allrs1057517822
SNPshotrs1057517822
SNPdbers1057517822
MSV3drs1057517822
GWAS Ctlgrs1057517822
Max Magnitude0
ClinVar
Risk rs1057517822(A;A)
Alt rs1057517822(A;A)
Reference Rs1057517822(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SLC2A1
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.43396395C>T
CLNSRC
CLNACC RCV000414747.1,