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rs587777513

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777513(A;A)
Make rs587777513(A;G)
ReferenceGRCh38 38.1/142
Chromosome4
Position150583174
GeneLRBA, MAB21L2
is asnp
is mentioned by
dbSNPrs587777513
ebirs587777513
HLIrs587777513
Exacrs587777513
Varsomers587777513
Maprs587777513
PheGenIrs587777513
hapmaprs587777513
1000 genomesrs587777513
hgdprs587777513
ensemblrs587777513
gopubmedrs587777513
geneviewrs587777513
scholarrs587777513
googlers587777513
pharmgkbrs587777513
gwascentralrs587777513
openSNPrs587777513
23andMers587777513
23andMe allrs587777513
SNP Nexus

SNPshotrs587777513
SNPdbers587777513
MSV3drs587777513
GWAS Ctlgrs587777513
Max Magnitude0
ClinVar
Risk rs587777513(A;A)
Alt rs587777513(A;A)
Reference rs587777513(G;G)
Significance Other
Disease Microphthalmia
Variation info
Gene MAB21L2 LRBA
CLNDBN Microphthalmia, syndromic 14
Reversed 0
HGVS NC_000004.11:g.151504326G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000128565.2,