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

rs61754436

From SNPedia

Orientationminus
Geno Mag Summary
(GA;GA) 0 common in clinvar
Make rs61754436(-;-)
Make rs61754436(-;GA)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154032394
GeneMECP2
is asnp
is mentioned by
dbSNPrs61754436
ebirs61754436
HLIrs61754436
Exacrs61754436
Varsomers61754436
Maprs61754436
PheGenIrs61754436
hapmaprs61754436
1000 genomesrs61754436
hgdprs61754436
ensemblrs61754436
gopubmedrs61754436
geneviewrs61754436
scholarrs61754436
googlers61754436
pharmgkbrs61754436
gwascentralrs61754436
openSNPrs61754436
23andMers61754436
23andMe allrs61754436
SNP Nexus

SNPshotrs61754436
SNPdbers61754436
MSV3drs61754436
GWAS Ctlgrs61754436
Max Magnitude0
ClinVar
Risk rs61754436(;)
Alt rs61754436(;)
Reference rs61754436(GA;GA)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153297845_153297846delTC
CLNSRC
CLNACC RCV000133028.2,