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rs267608388

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267608388(C;T)
Make rs267608388(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position154032241
GeneMECP2
is asnp
is mentioned by
dbSNPrs267608388
dbSNP (classic)rs267608388
ClinGenrs267608388
ebirs267608388
HLIrs267608388
Exacrs267608388
Gnomadrs267608388
Varsomers267608388
LitVarrs267608388
Maprs267608388
PheGenIrs267608388
Biobankrs267608388
1000 genomesrs267608388
hgdprs267608388
ensemblrs267608388
geneviewrs267608388
scholarrs267608388
googlers267608388
pharmgkbrs267608388
gwascentralrs267608388
openSNPrs267608388
23andMers267608388
23andMe allrs267608388
SNPshotrs267608388
SNPdbers267608388
MSV3drs267608388
GWAS Ctlgrs267608388
Max Magnitude0
ClinVar
Risk rs267608388(T;T)
Alt rs267608388(T;T)
Reference Rs267608388(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MECP2
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.153297692G>A
CLNSRC
CLNACC RCV000133074.4,