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rs267608530

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267608530(-;-)
Make rs267608530(-;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154031009
GeneMECP2
is asnp
is mentioned by
dbSNPrs267608530
ebirs267608530
HLIrs267608530
Exacrs267608530
Varsomers267608530
Maprs267608530
PheGenIrs267608530
hapmaprs267608530
1000 genomesrs267608530
hgdprs267608530
ensemblrs267608530
gopubmedrs267608530
geneviewrs267608530
scholarrs267608530
googlers267608530
pharmgkbrs267608530
gwascentralrs267608530
openSNPrs267608530
23andMers267608530
23andMe allrs267608530
SNP Nexus

SNPshotrs267608530
SNPdbers267608530
MSV3drs267608530
GWAS Ctlgrs267608530
Max Magnitude0
ClinVar
Risk rs267608530(;)
Alt rs267608530(;)
Reference rs267608530(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene MECP2
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.153296460delC
CLNSRC
CLNACC RCV000133249.2,