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rs1057517886

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057517886(A;T)
Make rs1057517886(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position88139174
GeneCEP290
is asnp
is mentioned by
dbSNPrs1057517886
dbSNP (classic)rs1057517886
ClinGenrs1057517886
ebirs1057517886
HLIrs1057517886
Exacrs1057517886
Gnomadrs1057517886
Varsomers1057517886
LitVarrs1057517886
Maprs1057517886
PheGenIrs1057517886
Biobankrs1057517886
1000 genomesrs1057517886
hgdprs1057517886
ensemblrs1057517886
geneviewrs1057517886
scholarrs1057517886
googlers1057517886
pharmgkbrs1057517886
gwascentralrs1057517886
openSNPrs1057517886
23andMers1057517886
23andMe allrs1057517886
SNPshotrs1057517886
SNPdbers1057517886
MSV3drs1057517886
GWAS Ctlgrs1057517886
Max Magnitude0
ClinVar
Risk rs1057517886(T;T)
Alt rs1057517886(T;T)
Reference Rs1057517886(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CEP290
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.88532951T>A
CLNSRC
CLNACC RCV000413097.1,