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rs587776457

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587776457(A;T)
Make rs587776457(T;T)
ReferenceGRCh38 38.1/142
ChromosomeX
Position153930761
GeneNAA10
is asnp
is mentioned by
dbSNPrs587776457
ebirs587776457
HLIrs587776457
Exacrs587776457
Varsomers587776457
Maprs587776457
PheGenIrs587776457
hapmaprs587776457
1000 genomesrs587776457
hgdprs587776457
ensemblrs587776457
gopubmedrs587776457
geneviewrs587776457
scholarrs587776457
googlers587776457
pharmgkbrs587776457
gwascentralrs587776457
openSNPrs587776457
23andMers587776457
23andMe allrs587776457
SNP Nexus

SNPshotrs587776457
SNPdbers587776457
MSV3drs587776457
GWAS Ctlgrs587776457
Max Magnitude0
ClinVar
Risk rs587776457(T;T)
Alt rs587776457(T;T)
Reference rs587776457(A;A)
Significance Pathogenic
Disease Lenz microphthalmia syndrome
Variation info
Gene NAA10
CLNDBN Lenz microphthalmia syndrome
Reversed 0
HGVS NC_000023.10:g.153196214A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000088650.3,