Have questions? Visit https://www.reddit.com/r/SNPedia

rs587777261

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(G;G) 0 common in clinvar
Make rs587777261(A;A)
Make rs587777261(A;G)
ReferenceGRCh38 38.1/142
ChromosomeX
Position53248133
GeneIQSEC2
is asnp
is mentioned by
dbSNPrs587777261
ebirs587777261
HLIrs587777261
Exacrs587777261
Varsomers587777261
Maprs587777261
PheGenIrs587777261
hapmaprs587777261
1000 genomesrs587777261
hgdprs587777261
ensemblrs587777261
gopubmedrs587777261
geneviewrs587777261
scholarrs587777261
googlers587777261
pharmgkbrs587777261
gwascentralrs587777261
openSNPrs587777261
23andMers587777261
23andMe allrs587777261
SNP Nexus

SNPshotrs587777261
SNPdbers587777261
MSV3drs587777261
GWAS Ctlgrs587777261
Max Magnitude0
ClinVar
Risk rs587777261(A,G;A,G)
Alt rs587777261(A,G;A,G)
Reference rs587777261(C;C)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene IQSEC2
CLNDBN Mental retardation, X-linked 1
Reversed 1
HGVS NC_000023.10:g.53277315G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000114357.2,