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rs587777511

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777511(A;A)
Make rs587777511(A;G)
ReferenceGRCh38 38.1/142
Chromosome4
Position150583181
GeneLRBA, MAB21L2
is asnp
is mentioned by
dbSNPrs587777511
ebirs587777511
HLIrs587777511
Exacrs587777511
Varsomers587777511
Maprs587777511
PheGenIrs587777511
hapmaprs587777511
1000 genomesrs587777511
hgdprs587777511
ensemblrs587777511
gopubmedrs587777511
geneviewrs587777511
scholarrs587777511
googlers587777511
pharmgkbrs587777511
gwascentralrs587777511
openSNPrs587777511
23andMers587777511
23andMe allrs587777511
SNP Nexus

SNPshotrs587777511
SNPdbers587777511
MSV3drs587777511
GWAS Ctlgrs587777511
Max Magnitude0
ClinVar
Risk rs587777511(A;A)
Alt rs587777511(A;A)
Reference rs587777511(G;G)
Significance Other
Disease Microphthalmia
Variation info
Gene MAB21L2 LRBA
CLNDBN Microphthalmia, syndromic 14
Reversed 0
HGVS NC_000004.11:g.151504333G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000128563.2,