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rs267607221

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607221(A;A)
Make rs267607221(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position46899455
GeneLRP4
is asnp
is mentioned by
dbSNPrs267607221
ebirs267607221
HLIrs267607221
Exacrs267607221
Varsomers267607221
Maprs267607221
PheGenIrs267607221
hapmaprs267607221
1000 genomesrs267607221
hgdprs267607221
ensemblrs267607221
gopubmedrs267607221
geneviewrs267607221
scholarrs267607221
googlers267607221
pharmgkbrs267607221
gwascentralrs267607221
openSNPrs267607221
23andMers267607221
23andMe allrs267607221
SNP Nexus

SNPshotrs267607221
SNPdbers267607221
MSV3drs267607221
GWAS Ctlgrs267607221
Max Magnitude0
ClinVar
Risk rs267607221(A;A)
Alt rs267607221(A;A)
Reference rs267607221(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.46921006C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000006044.2,