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rs267607223

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs267607223(A;C)
Make rs267607223(C;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position46894748
GeneLRP4
is asnp
is mentioned by
dbSNPrs267607223
ebirs267607223
HLIrs267607223
Exacrs267607223
Varsomers267607223
Maprs267607223
PheGenIrs267607223
hapmaprs267607223
1000 genomesrs267607223
hgdprs267607223
ensemblrs267607223
gopubmedrs267607223
geneviewrs267607223
scholarrs267607223
googlers267607223
pharmgkbrs267607223
gwascentralrs267607223
openSNPrs267607223
23andMers267607223
23andMe allrs267607223
SNP Nexus

SNPshotrs267607223
SNPdbers267607223
MSV3drs267607223
GWAS Ctlgrs267607223
Max Magnitude0
ClinVar
Risk rs267607223(C;C)
Alt rs267607223(C;C)
Reference rs267607223(A;A)
Significance Pathogenic
Disease Syndactyly Cenani Lenz type
Variation info
Gene LRP4
CLNDBN Syndactyly Cenani Lenz type
Reversed 1
HGVS NC_000011.9:g.46916299T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000006046.2,