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rs1057519165

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057519165(-;-)
Make rs1057519165(-;A)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position88060836
GeneCEP290
is asnp
is mentioned by
dbSNPrs1057519165
dbSNP (old)rs1057519165
ClinGenrs1057519165
ebirs1057519165
HLIrs1057519165
Exacrs1057519165
Gnomadrs1057519165
Varsomers1057519165
Maprs1057519165
PheGenIrs1057519165
Biobankrs1057519165
1000 genomesrs1057519165
hgdprs1057519165
ensemblrs1057519165
gopubmedrs1057519165
geneviewrs1057519165
scholarrs1057519165
googlers1057519165
pharmgkbrs1057519165
gwascentralrs1057519165
openSNPrs1057519165
23andMers1057519165
23andMe allrs1057519165
SNPshotrs1057519165
SNPdbers1057519165
MSV3drs1057519165
GWAS Ctlgrs1057519165
Max Magnitude0
ClinVar
Risk rs1057519165(-;-)
Alt rs1057519165(-;-)
Reference Rs1057519165(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CEP290
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.88454613delT
CLNSRC
CLNACC RCV000415838.1,