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rs875989838

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs875989838(-;-)
Make rs875989838(-;C)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position190120435
GeneP3H2, P3H2-AS1
is asnp
is mentioned by
dbSNPrs875989838
ebirs875989838
HLIrs875989838
Exacrs875989838
Varsomers875989838
Maprs875989838
PheGenIrs875989838
hapmaprs875989838
1000 genomesrs875989838
hgdprs875989838
ensemblrs875989838
gopubmedrs875989838
geneviewrs875989838
scholarrs875989838
googlers875989838
pharmgkbrs875989838
gwascentralrs875989838
openSNPrs875989838
23andMers875989838
23andMe allrs875989838
SNP Nexus

SNPshotrs875989838
SNPdbers875989838
MSV3drs875989838
GWAS Ctlgrs875989838
Max Magnitude0
ClinVar
Risk rs875989838(;)
Alt rs875989838(;)
Reference rs875989838(C;C)
Significance Pathogenic
Disease Myopia
Variation info
Gene LOC101929152 LEPREL1 P3H2-AS1
CLNDBN Myopia, high, with cataract and vitreoretinal degeneration
Reversed 1
HGVS NC_000003.11:g.189838224delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000210936.1,