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rs587779752

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587779752(C;T)
Make rs587779752(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position156791474
GeneLMBR1
is asnp
is mentioned by
dbSNPrs587779752
ebirs587779752
HLIrs587779752
Exacrs587779752
Varsomers587779752
Maprs587779752
PheGenIrs587779752
hapmaprs587779752
1000 genomesrs587779752
hgdprs587779752
ensemblrs587779752
gopubmedrs587779752
geneviewrs587779752
scholarrs587779752
googlers587779752
pharmgkbrs587779752
gwascentralrs587779752
openSNPrs587779752
23andMers587779752
23andMe allrs587779752
SNP Nexus

SNPshotrs587779752
SNPdbers587779752
MSV3drs587779752
GWAS Ctlgrs587779752
Max Magnitude0
ClinVar
Risk rs587779752(T;T)
Alt rs587779752(T;T)
Reference rs587779752(C;C)
Significance Pathogenic
Disease Triphalangeal thumb Polydactyly Tibia
Variation info
Gene LMBR1
CLNDBN Triphalangeal thumb Polydactyly, preaxial II Tibia, hypoplasia or aplasia of, with polydactyly
Reversed 1
HGVS NC_000007.13:g.156584168G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000148023.3, RCV000148024.3, RCV000148025.4,