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rs1057517738

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057517738(C;C)
Make rs1057517738(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position33068818
GeneGLB1
is asnp
is mentioned by
dbSNPrs1057517738
dbSNP (classic)rs1057517738
ClinGenrs1057517738
ebirs1057517738
HLIrs1057517738
Exacrs1057517738
Gnomadrs1057517738
Varsomers1057517738
LitVarrs1057517738
Maprs1057517738
PheGenIrs1057517738
Biobankrs1057517738
1000 genomesrs1057517738
hgdprs1057517738
ensemblrs1057517738
geneviewrs1057517738
scholarrs1057517738
googlers1057517738
pharmgkbrs1057517738
gwascentralrs1057517738
openSNPrs1057517738
23andMers1057517738
23andMe allrs1057517738
SNPshotrs1057517738
SNPdbers1057517738
MSV3drs1057517738
GWAS Ctlgrs1057517738
Max Magnitude0
ClinVar
Risk rs1057517738(C;C)
Alt rs1057517738(C;C)
Reference Rs1057517738(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene GLB1
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.33110310A>G
CLNSRC
CLNACC RCV000414347.1,