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rs587777479

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587777479(A;G)
Make rs587777479(G;G)
ReferenceGRCh38 38.1/142
Chromosome2
Position5693068
GeneLINC01248, SOX11
is asnp
is mentioned by
dbSNPrs587777479
ebirs587777479
HLIrs587777479
Exacrs587777479
Varsomers587777479
Maprs587777479
PheGenIrs587777479
hapmaprs587777479
1000 genomesrs587777479
hgdprs587777479
ensemblrs587777479
gopubmedrs587777479
geneviewrs587777479
scholarrs587777479
googlers587777479
pharmgkbrs587777479
gwascentralrs587777479
openSNPrs587777479
23andMers587777479
23andMe allrs587777479
SNP Nexus

SNPshotrs587777479
SNPdbers587777479
MSV3drs587777479
GWAS Ctlgrs587777479
Max Magnitude0
ClinVar
Risk rs587777479(G;G)
Alt rs587777479(G;G)
Reference rs587777479(A;A)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene LINC01248 SOX11
CLNDBN Mental retardation, autosomal dominant 27
Reversed 0
HGVS NC_000002.11:g.5833200A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000128428.3,