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rs786205216

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205216(-;-)
Make rs786205216(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position3532214
GeneLRPAP1
is asnp
is mentioned by
dbSNPrs786205216
ebirs786205216
HLIrs786205216
Exacrs786205216
Varsomers786205216
Maprs786205216
PheGenIrs786205216
hapmaprs786205216
1000 genomesrs786205216
hgdprs786205216
ensemblrs786205216
gopubmedrs786205216
geneviewrs786205216
scholarrs786205216
googlers786205216
pharmgkbrs786205216
gwascentralrs786205216
openSNPrs786205216
23andMers786205216
23andMe allrs786205216
SNP Nexus

SNPshotrs786205216
SNPdbers786205216
MSV3drs786205216
GWAS Ctlgrs786205216
Max Magnitude0
ClinVar
Risk rs786205216(;)
Alt rs786205216(;)
Reference rs786205216(C;C)
Significance Pathogenic
Disease Myopia 23
Variation info
Gene LRPAP1
CLNDBN Myopia 23, autosomal recessive
Reversed 1
HGVS NC_000004.11:g.3533941delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000170452.3,