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rs863224855

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863224855(A;T)
Make rs863224855(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position181566061
GeneCERKL
is asnp
is mentioned by
dbSNPrs863224855
ebirs863224855
HLIrs863224855
Exacrs863224855
Varsomers863224855
Maprs863224855
PheGenIrs863224855
hapmaprs863224855
1000 genomesrs863224855
hgdprs863224855
ensemblrs863224855
gopubmedrs863224855
geneviewrs863224855
scholarrs863224855
googlers863224855
pharmgkbrs863224855
gwascentralrs863224855
openSNPrs863224855
23andMers863224855
23andMe allrs863224855
SNP Nexus

SNPshotrs863224855
SNPdbers863224855
MSV3drs863224855
GWAS Ctlgrs863224855
Max Magnitude0
ClinVar
Risk rs863224855(T;T)
Alt rs863224855(T;T)
Reference rs863224855(A;A)
Significance Pathogenic
Disease Retinitis pigmentosa 26
Variation info
Gene CERKL
CLNDBN Retinitis pigmentosa 26
Reversed 1
HGVS NC_000002.11:g.182430788T>A
CLNSRC
CLNACC RCV000196604.1,