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

rs61752365

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs61752365(C;G)
Make rs61752365(G;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154030790
GeneMECP2
is asnp
is mentioned by
dbSNPrs61752365
ebirs61752365
HLIrs61752365
Exacrs61752365
Varsomers61752365
Maprs61752365
PheGenIrs61752365
hapmaprs61752365
1000 genomesrs61752365
hgdprs61752365
ensemblrs61752365
gopubmedrs61752365
geneviewrs61752365
scholarrs61752365
googlers61752365
pharmgkbrs61752365
gwascentralrs61752365
openSNPrs61752365
23andMers61752365
23andMe allrs61752365
SNP Nexus

SNPshotrs61752365
SNPdbers61752365
MSV3drs61752365
GWAS Ctlgrs61752365
Max Magnitude0
ClinVar
Risk rs61752365(G;G)
Alt rs61752365(G;G)
Reference rs61752365(C;C)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296241G>C
CLNSRC
CLNACC RCV000132834.2,