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

rs61749728

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs61749728(-;-)
Make rs61749728(-;T)
Make rs61749728(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154031207
GeneMECP2
is asnp
is mentioned by
dbSNPrs61749728
ebirs61749728
HLIrs61749728
Exacrs61749728
Varsomers61749728
Maprs61749728
PheGenIrs61749728
hapmaprs61749728
1000 genomesrs61749728
hgdprs61749728
ensemblrs61749728
gopubmedrs61749728
geneviewrs61749728
scholarrs61749728
googlers61749728
pharmgkbrs61749728
gwascentralrs61749728
openSNPrs61749728
23andMers61749728
23andMe allrs61749728
SNP Nexus

SNPshotrs61749728
SNPdbers61749728
MSV3drs61749728
GWAS Ctlgrs61749728
Max Magnitude0
ClinVar
Risk rs61749728(T;T)
Alt rs61749728(T;T)
Reference rs61749728(;)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296659dupA
CLNSRC
CLNACC RCV000133180.2,