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rs139574075

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs139574075(A;A)
Make rs139574075(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position15453899
GeneCOLQ
is asnp
is mentioned by
dbSNPrs139574075
dbSNP (old)rs139574075
ClinGenrs139574075
ebirs139574075
HLIrs139574075
Exacrs139574075
Gnomadrs139574075
Varsomers139574075
Maprs139574075
PheGenIrs139574075
Biobankrs139574075
1000 genomesrs139574075
hgdprs139574075
ensemblrs139574075
gopubmedrs139574075
geneviewrs139574075
scholarrs139574075
googlers139574075
pharmgkbrs139574075
gwascentralrs139574075
openSNPrs139574075
23andMers139574075
23andMe allrs139574075
SNPshotrs139574075
SNPdbers139574075
MSV3drs139574075
GWAS Ctlgrs139574075
Max Magnitude0
ClinVar
Risk rs139574075(A;A) rs139574075(T;T)
Alt rs139574075(A;A) rs139574075(T;T)
Reference Rs139574075(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene COLQ
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.15495406G>A
CLNSRC
CLNACC RCV000443300.1,