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rs267607222

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607222(A;A)
Make rs267607222(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position46899884
GeneLRP4
is asnp
is mentioned by
dbSNPrs267607222
ebirs267607222
HLIrs267607222
Exacrs267607222
Varsomers267607222
Maprs267607222
PheGenIrs267607222
hapmaprs267607222
1000 genomesrs267607222
hgdprs267607222
ensemblrs267607222
gopubmedrs267607222
geneviewrs267607222
scholarrs267607222
googlers267607222
pharmgkbrs267607222
gwascentralrs267607222
openSNPrs267607222
23andMers267607222
23andMe allrs267607222
SNP Nexus

SNPshotrs267607222
SNPdbers267607222
MSV3drs267607222
GWAS Ctlgrs267607222
Max Magnitude0
ClinVar
Risk rs267607222(A;A)
Alt rs267607222(A;A)
Reference rs267607222(G;G)
Significance Pathogenic
Disease Syndactyly Cenani Lenz type
Variation info
Gene LRP4
CLNDBN Syndactyly Cenani Lenz type
Reversed 1
HGVS NC_000011.9:g.46921435C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000006041.2,