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rs398122836

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TC;TC) 0 common in clinvar
Make rs398122836(-;-)
Make rs398122836(-;TC)
ReferenceGRCh38 38.1/141
Chromosome4
Position3514899
GeneLRPAP1
is asnp
is mentioned by
dbSNPrs398122836
ebirs398122836
HLIrs398122836
Exacrs398122836
Varsomers398122836
Maprs398122836
PheGenIrs398122836
hapmaprs398122836
1000 genomesrs398122836
hgdprs398122836
ensemblrs398122836
gopubmedrs398122836
geneviewrs398122836
scholarrs398122836
googlers398122836
pharmgkbrs398122836
gwascentralrs398122836
openSNPrs398122836
23andMers398122836
23andMe allrs398122836
SNP Nexus

SNPshotrs398122836
SNPdbers398122836
MSV3drs398122836
GWAS Ctlgrs398122836
Max Magnitude0
ClinVar
Risk rs398122836(;)
Alt rs398122836(;)
Reference rs398122836(TC;TC)
Significance Pathogenic
Disease Myopia 23
Variation info
Gene LRPAP1
CLNDBN Myopia 23, autosomal recessive
Reversed 1
HGVS NC_000004.11:g.3516626_3516627delGA
CLNSRC OMIM Allelic Variant
CLNACC RCV000055655.27,