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

rs786205040

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205040(C;GA)
Make rs786205040(GA;GA)
ReferenceGRCh38.p2 38.2/146
ChromosomeX
Position154097636
GeneMECP2
is asnp
is mentioned by
dbSNPrs786205040
ebirs786205040
HLIrs786205040
Exacrs786205040
Varsomers786205040
Maprs786205040
PheGenIrs786205040
hapmaprs786205040
1000 genomesrs786205040
hgdprs786205040
ensemblrs786205040
gopubmedrs786205040
geneviewrs786205040
scholarrs786205040
googlers786205040
pharmgkbrs786205040
gwascentralrs786205040
openSNPrs786205040
23andMers786205040
23andMe allrs786205040
SNP Nexus

SNPshotrs786205040
SNPdbers786205040
MSV3drs786205040
GWAS Ctlgrs786205040
Max Magnitude0
ClinVar
Risk rs786205040(GA;GA)
Alt rs786205040(GA;GA)
Reference rs786205040(C;C)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153363093delGinsTC
CLNSRC
CLNACC RCV000170285.1,