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rs1057521153

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057521153(C;C)
Make rs1057521153(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position15456524
GeneCOLQ
is asnp
is mentioned by
dbSNPrs1057521153
dbSNP (old)rs1057521153
ClinGenrs1057521153
ebirs1057521153
HLIrs1057521153
Exacrs1057521153
Gnomadrs1057521153
Varsomers1057521153
LitVarrs1057521153
Maprs1057521153
PheGenIrs1057521153
Biobankrs1057521153
1000 genomesrs1057521153
hgdprs1057521153
ensemblrs1057521153
gopubmedrs1057521153
geneviewrs1057521153
scholarrs1057521153
googlers1057521153
pharmgkbrs1057521153
gwascentralrs1057521153
openSNPrs1057521153
23andMers1057521153
23andMe allrs1057521153
SNPshotrs1057521153
SNPdbers1057521153
MSV3drs1057521153
GWAS Ctlgrs1057521153
Max Magnitude0
ClinVar
Risk rs1057521153(C;C)
Alt rs1057521153(C;C)
Reference Rs1057521153(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene COLQ
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.15498031A>G
CLNSRC
CLNACC RCV000426405.1,