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rs587777172

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587777172(C;T)
Make rs587777172(T;T)
ReferenceGRCh38 38.1/142
Chromosome1
Position225403403
GeneLBR
is asnp
is mentioned by
dbSNPrs587777172
ebirs587777172
HLIrs587777172
Exacrs587777172
Varsomers587777172
Maprs587777172
PheGenIrs587777172
hapmaprs587777172
1000 genomesrs587777172
hgdprs587777172
ensemblrs587777172
gopubmedrs587777172
geneviewrs587777172
scholarrs587777172
googlers587777172
pharmgkbrs587777172
gwascentralrs587777172
openSNPrs587777172
23andMers587777172
23andMe allrs587777172
SNP Nexus

SNPshotrs587777172
SNPdbers587777172
MSV3drs587777172
GWAS Ctlgrs587777172
Max Magnitude0
ClinVar
Risk rs587777172(A,T;A,T)
Alt rs587777172(A,T;A,T)
Reference rs587777172(C;C)
Significance Pathogenic
Disease Greenberg dysplasia
Variation info
Gene LBR
CLNDBN Greenberg dysplasia
Reversed 0
HGVS NC_000001.10:g.225591105C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000087264.3,