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rs267608514

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs267608514(-;-)
Make rs267608514(-;A)
Make rs267608514(A;A)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154031151
GeneMECP2
is asnp
is mentioned by
dbSNPrs267608514
ebirs267608514
HLIrs267608514
Exacrs267608514
Varsomers267608514
Maprs267608514
PheGenIrs267608514
hapmaprs267608514
1000 genomesrs267608514
hgdprs267608514
ensemblrs267608514
gopubmedrs267608514
geneviewrs267608514
scholarrs267608514
googlers267608514
pharmgkbrs267608514
gwascentralrs267608514
openSNPrs267608514
23andMers267608514
23andMe allrs267608514
SNP Nexus

SNPshotrs267608514
SNPdbers267608514
MSV3drs267608514
GWAS Ctlgrs267608514
Max Magnitude0
ClinVar
Risk rs267608514(A;A)
Alt rs267608514(A;A)
Reference rs267608514(;)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296602_153296603insT
CLNSRC
CLNACC RCV000133195.2,