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rs375548374

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs375548374(A;A)
Make rs375548374(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position88053733
GeneCEP290
is asnp
is mentioned by
dbSNPrs375548374
dbSNP (classic)rs375548374
ClinGenrs375548374
ebirs375548374
HLIrs375548374
Exacrs375548374
Gnomadrs375548374
Varsomers375548374
LitVarrs375548374
Maprs375548374
PheGenIrs375548374
Biobankrs375548374
1000 genomesrs375548374
hgdprs375548374
ensemblrs375548374
geneviewrs375548374
scholarrs375548374
googlers375548374
pharmgkbrs375548374
gwascentralrs375548374
openSNPrs375548374
23andMers375548374
SNPshotrs375548374
SNPdbers375548374
MSV3drs375548374
GWAS Ctlgrs375548374
Max Magnitude0
ClinVar
Risk rs375548374(A;A) rs375548374(T;T)
Alt rs375548374(A;A) rs375548374(T;T)
Reference Rs375548374(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CEP290
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.88447510G>T
CLNSRC
CLNACC RCV000415801.1,