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rs267608559

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AAGACCTGTAAGAGCCCTG;AAGACCTGTAAGAGCCCTG) 0 common in clinvar
Make rs267608559(-;-)
Make rs267608559(-;AAGACCTGTAAGAGCCCTG)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154030801
GeneMECP2
is asnp
is mentioned by
dbSNPrs267608559
dbSNP (old)rs267608559
ClinGenrs267608559
ebirs267608559
HLIrs267608559
Exacrs267608559
Gnomadrs267608559
Varsomers267608559
Maprs267608559
PheGenIrs267608559
Biobankrs267608559
1000 genomesrs267608559
hgdprs267608559
ensemblrs267608559
gopubmedrs267608559
geneviewrs267608559
scholarrs267608559
googlers267608559
pharmgkbrs267608559
gwascentralrs267608559
openSNPrs267608559
23andMers267608559
23andMe allrs267608559
SNP Nexus

SNPshotrs267608559
SNPdbers267608559
MSV3drs267608559
GWAS Ctlgrs267608559
Max Magnitude0
ClinVar
Risk rs267608559(-;-)
Alt rs267608559(-;-)
Reference Rs267608559(AAGACCTGTAAGAGCCCTG;AAGACCTGTAAGAGCCCTG)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296252_153296270del19
CLNSRC
CLNACC RCV000132827.2,