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rs267608568

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267608568(-;-)
Make rs267608568(-;C)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154030723
GeneMECP2
is asnp
is mentioned by
dbSNPrs267608568
ebirs267608568
HLIrs267608568
Exacrs267608568
Varsomers267608568
Maprs267608568
PheGenIrs267608568
hapmaprs267608568
1000 genomesrs267608568
hgdprs267608568
ensemblrs267608568
gopubmedrs267608568
geneviewrs267608568
scholarrs267608568
googlers267608568
pharmgkbrs267608568
gwascentralrs267608568
openSNPrs267608568
23andMers267608568
23andMe allrs267608568
SNP Nexus

SNPshotrs267608568
SNPdbers267608568
MSV3drs267608568
GWAS Ctlgrs267608568
Max Magnitude0
ClinVar
Risk rs267608568(;)
Alt rs267608568(;)
Reference rs267608568(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MECP2
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.153296174delG
CLNSRC
CLNACC RCV000132858.2,