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rs587778875

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs587778875(-;C)
Make rs587778875(C;C)
ReferenceGRCh38.p7 38.3/149
Chromosome2
Position38074520
GeneCYP1B1
is asnp
is mentioned by
dbSNPrs587778875
dbSNP (classic)rs587778875
ClinGenrs587778875
ebirs587778875
HLIrs587778875
Exacrs587778875
Gnomadrs587778875
Varsomers587778875
LitVarrs587778875
Maprs587778875
PheGenIrs587778875
Biobankrs587778875
1000 genomesrs587778875
hgdprs587778875
ensemblrs587778875
geneviewrs587778875
scholarrs587778875
googlers587778875
pharmgkbrs587778875
gwascentralrs587778875
openSNPrs587778875
23andMers587778875
SNPshotrs587778875
SNPdbers587778875
MSV3drs587778875
GWAS Ctlgrs587778875
Max Magnitude0
ClinVar
Risk rs587778875(C;C)
Alt rs587778875(C;C)
Reference Rs587778875(-;-)
Significance Pathogenic
Disease Coloboma not provided
Variation info
Gene CYP1B1
CLNDBN Coloboma not provided
Reversed 1
HGVS NC_000002.11:g.38301664dupG
CLNSRC
CLNACC RCV000059339.2, RCV000363659.1,