Have questions? Visit https://www.reddit.com/r/SNPedia

rs786205023

From SNPedia

Orientationminus
Geno Mag Summary
(AACA;AACA) 0 common in clinvar
Make rs786205023(AACA;TG)
Make rs786205023(TG;TG)
ReferenceGRCh38.p2 38.2/146
ChromosomeX
Position154030417
GeneMECP2
is asnp
is mentioned by
dbSNPrs786205023
ebirs786205023
HLIrs786205023
Exacrs786205023
Varsomers786205023
Maprs786205023
PheGenIrs786205023
hapmaprs786205023
1000 genomesrs786205023
hgdprs786205023
ensemblrs786205023
gopubmedrs786205023
geneviewrs786205023
scholarrs786205023
googlers786205023
pharmgkbrs786205023
gwascentralrs786205023
openSNPrs786205023
23andMers786205023
23andMe allrs786205023
SNP Nexus

SNPshotrs786205023
SNPdbers786205023
MSV3drs786205023
GWAS Ctlgrs786205023
Max Magnitude0
ClinVar
Risk rs786205023(TG;TG)
Alt rs786205023(TG;TG)
Reference rs786205023(AACA;AACA)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153295868_153295871delTGTTinsCA
CLNSRC
CLNACC RCV000170159.1,