Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057519245

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057519245(A;A)
Make rs1057519245(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position88089032
GeneCEP290
is asnp
is mentioned by
dbSNPrs1057519245
dbSNP (old)rs1057519245
ClinGenrs1057519245
ebirs1057519245
HLIrs1057519245
Exacrs1057519245
Gnomadrs1057519245
Varsomers1057519245
Maprs1057519245
PheGenIrs1057519245
Biobankrs1057519245
1000 genomesrs1057519245
hgdprs1057519245
ensemblrs1057519245
gopubmedrs1057519245
geneviewrs1057519245
scholarrs1057519245
googlers1057519245
pharmgkbrs1057519245
gwascentralrs1057519245
openSNPrs1057519245
23andMers1057519245
23andMe allrs1057519245
SNPshotrs1057519245
SNPdbers1057519245
MSV3drs1057519245
GWAS Ctlgrs1057519245
Max Magnitude0
ClinVar
Risk rs1057519245(A;A)
Alt rs1057519245(A;A)
Reference Rs1057519245(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CEP290
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.88482809C>T
CLNSRC
CLNACC RCV000416190.1,