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rs587776755

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(G;G) 0 common in clinvar
Make rs587776755(C;G)
ReferenceGRCh38 38.1/142
ChromosomeX
Position20195146
GeneRPS6KA3
is asnp
is mentioned by
dbSNPrs587776755
ebirs587776755
HLIrs587776755
Exacrs587776755
Varsomers587776755
Maprs587776755
PheGenIrs587776755
hapmaprs587776755
1000 genomesrs587776755
hgdprs587776755
ensemblrs587776755
gopubmedrs587776755
geneviewrs587776755
scholarrs587776755
googlers587776755
pharmgkbrs587776755
gwascentralrs587776755
openSNPrs587776755
23andMers587776755
23andMe allrs587776755
SNP Nexus

SNPshotrs587776755
SNPdbers587776755
MSV3drs587776755
GWAS Ctlgrs587776755
Max Magnitude0
ClinVar
Risk rs587776755(C;C)
Alt rs587776755(C;C)
Reference rs587776755(G;G)
Significance Pathogenic
Disease Coffin-Lowry syndrome
Variation info
Gene RPS6KA3
CLNDBN Coffin-Lowry syndrome
Reversed 1
HGVS NC_000023.10:g.20213264C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000012420.23,