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rs267608489

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267608489(-;-)
Make rs267608489(-;C)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154031333
GeneMECP2
is asnp
is mentioned by
dbSNPrs267608489
ebirs267608489
HLIrs267608489
Exacrs267608489
Varsomers267608489
Maprs267608489
PheGenIrs267608489
hapmaprs267608489
1000 genomesrs267608489
hgdprs267608489
ensemblrs267608489
gopubmedrs267608489
geneviewrs267608489
scholarrs267608489
googlers267608489
pharmgkbrs267608489
gwascentralrs267608489
openSNPrs267608489
23andMers267608489
23andMe allrs267608489
SNP Nexus

SNPshotrs267608489
SNPdbers267608489
MSV3drs267608489
GWAS Ctlgrs267608489
Max Magnitude0
ClinVar
Risk rs267608489(;)
Alt rs267608489(;)
Reference rs267608489(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MECP2
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.153296784delG
CLNSRC
CLNACC RCV000133141.2,