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rs786205127

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786205127(-;-)
Make rs786205127(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position3518180
GeneLRPAP1
is asnp
is mentioned by
dbSNPrs786205127
ebirs786205127
HLIrs786205127
Exacrs786205127
Varsomers786205127
Maprs786205127
PheGenIrs786205127
hapmaprs786205127
1000 genomesrs786205127
hgdprs786205127
ensemblrs786205127
gopubmedrs786205127
geneviewrs786205127
scholarrs786205127
googlers786205127
pharmgkbrs786205127
gwascentralrs786205127
openSNPrs786205127
23andMers786205127
23andMe allrs786205127
SNP Nexus

SNPshotrs786205127
SNPdbers786205127
MSV3drs786205127
GWAS Ctlgrs786205127
Max Magnitude0
ClinVar
Risk rs786205127(;)
Alt rs786205127(;)
Reference rs786205127(A;A)
Significance Pathogenic
Disease Myopia 23
Variation info
Gene LRPAP1
CLNDBN Myopia 23, autosomal recessive
Reversed 1
HGVS NC_000004.11:g.3519907delT
CLNSRC OMIM Allelic Variant
CLNACC RCV000055654.27,