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rs863224894

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863224894(C;C)
Make rs863224894(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position112021424
GeneMERTK
is asnp
is mentioned by
dbSNPrs863224894
ebirs863224894
HLIrs863224894
Exacrs863224894
Varsomers863224894
Maprs863224894
PheGenIrs863224894
hapmaprs863224894
1000 genomesrs863224894
hgdprs863224894
ensemblrs863224894
gopubmedrs863224894
geneviewrs863224894
scholarrs863224894
googlers863224894
pharmgkbrs863224894
gwascentralrs863224894
openSNPrs863224894
23andMers863224894
23andMe allrs863224894
SNP Nexus

SNPshotrs863224894
SNPdbers863224894
MSV3drs863224894
GWAS Ctlgrs863224894
Max Magnitude0
ClinVar
Risk rs863224894(C;C)
Alt rs863224894(C;C)
Reference rs863224894(T;T)
Significance Probable-Pathogenic
Disease Retinitis pigmentosa 38
Variation info
Gene MERTK
CLNDBN Retinitis pigmentosa 38
Reversed 0
HGVS NC_000002.11:g.112779001T>C
CLNSRC
CLNACC RCV000197519.1,