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rs1057524868

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057524868(C;T)
Make rs1057524868(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position33014094
GeneGLB1
is asnp
is mentioned by
dbSNPrs1057524868
dbSNP (old)rs1057524868
ClinGenrs1057524868
ebirs1057524868
HLIrs1057524868
Exacrs1057524868
Gnomadrs1057524868
Varsomers1057524868
Maprs1057524868
PheGenIrs1057524868
Biobankrs1057524868
1000 genomesrs1057524868
hgdprs1057524868
ensemblrs1057524868
gopubmedrs1057524868
geneviewrs1057524868
scholarrs1057524868
googlers1057524868
pharmgkbrs1057524868
gwascentralrs1057524868
openSNPrs1057524868
23andMers1057524868
23andMe allrs1057524868
SNPshotrs1057524868
SNPdbers1057524868
MSV3drs1057524868
GWAS Ctlgrs1057524868
Max Magnitude0
ClinVar
Risk rs1057524868(T;T)
Alt rs1057524868(T;T)
Reference Rs1057524868(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GLB1
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.33055586G>A
CLNSRC
CLNACC RCV000422841.1,