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rs267608386

From SNPedia

Orientationminus
Geno Mag Summary
(AGAAAAGTCCTGG;AGAAAAGTCCTGG) 0 common in clinvar
Make rs267608386(-;-)
Make rs267608386(-;AGAAAAGTCCTGG)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154031175
GeneMECP2
is asnp
is mentioned by
dbSNPrs267608386
ebirs267608386
HLIrs267608386
Exacrs267608386
Varsomers267608386
Maprs267608386
PheGenIrs267608386
hapmaprs267608386
1000 genomesrs267608386
hgdprs267608386
ensemblrs267608386
gopubmedrs267608386
geneviewrs267608386
scholarrs267608386
googlers267608386
pharmgkbrs267608386
gwascentralrs267608386
openSNPrs267608386
23andMers267608386
23andMe allrs267608386
SNP Nexus

SNPshotrs267608386
SNPdbers267608386
MSV3drs267608386
GWAS Ctlgrs267608386
Max Magnitude0
ClinVar
Risk rs267608386(;)
Alt rs267608386(;)
Reference rs267608386(AGAAAAGTCCTGG;AGAAAAGTCCTGG)
Significance Probable-Pathogenic
Disease not provided Rett syndrome
Variation info
Gene MECP2
CLNDBN not provided Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296626_153296638delCCAGGACTTTTCT
CLNSRC
CLNACC RCV000133186.1, RCV000168686.1,