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rs786205049

From SNPedia

Orientationminus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs786205049(-;-)
Make rs786205049(-;TG)
ReferenceGRCh38.p2 38.2/146
ChromosomeX
Position154097601
GeneMECP2
is asnp
is mentioned by
dbSNPrs786205049
ebirs786205049
HLIrs786205049
Exacrs786205049
Varsomers786205049
Maprs786205049
PheGenIrs786205049
hapmaprs786205049
1000 genomesrs786205049
hgdprs786205049
ensemblrs786205049
gopubmedrs786205049
geneviewrs786205049
scholarrs786205049
googlers786205049
pharmgkbrs786205049
gwascentralrs786205049
openSNPrs786205049
23andMers786205049
23andMe allrs786205049
SNP Nexus

SNPshotrs786205049
SNPdbers786205049
MSV3drs786205049
GWAS Ctlgrs786205049
Max Magnitude0
ClinVar
Risk rs786205049(;)
Alt rs786205049(;)
Reference rs786205049(TG;TG)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153363058_153363059delCA
CLNSRC
CLNACC RCV000170295.2,