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rs587777514

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777514(A;A)
Make rs587777514(A;G)
ReferenceGRCh38 38.1/142
Chromosome4
Position150583769
GeneLRBA, MAB21L2
is asnp
is mentioned by
dbSNPrs587777514
ebirs587777514
HLIrs587777514
Exacrs587777514
Varsomers587777514
Maprs587777514
PheGenIrs587777514
hapmaprs587777514
1000 genomesrs587777514
hgdprs587777514
ensemblrs587777514
gopubmedrs587777514
geneviewrs587777514
scholarrs587777514
googlers587777514
pharmgkbrs587777514
gwascentralrs587777514
openSNPrs587777514
23andMers587777514
23andMe allrs587777514
SNP Nexus

SNPshotrs587777514
SNPdbers587777514
MSV3drs587777514
GWAS Ctlgrs587777514
Max Magnitude0
ClinVar
Risk rs587777514(A,T;A,T)
Alt rs587777514(A,T;A,T)
Reference rs587777514(G;G)
Significance Other
Disease Microphthalmia
Variation info
Gene MAB21L2 LRBA
CLNDBN Microphthalmia, syndromic 14
Reversed 0
HGVS NC_000004.11:g.151504921G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000128566.2,