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

rs56268439

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs56268439(C;T)
Make rs56268439(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154030639
GeneMECP2
is asnp
is mentioned by
dbSNPrs56268439
ebirs56268439
HLIrs56268439
Exacrs56268439
Varsomers56268439
Maprs56268439
PheGenIrs56268439
hapmaprs56268439
1000 genomesrs56268439
hgdprs56268439
ensemblrs56268439
gopubmedrs56268439
geneviewrs56268439
scholarrs56268439
googlers56268439
pharmgkbrs56268439
gwascentralrs56268439
openSNPrs56268439
23andMers56268439
23andMe allrs56268439
SNP Nexus

SNPshotrs56268439
SNPdbers56268439
MSV3drs56268439
GWAS Ctlgrs56268439
Max Magnitude0
ClinVar
Risk rs56268439(A,T;A,T)
Alt rs56268439(A,T;A,T)
Reference rs56268439(C;C)
Significance Pathogenic
Disease Rett syndrome not specified not provided
Variation info
Gene MECP2
CLNDBN Rett syndrome not specified not provided
Reversed 0
HGVS NC_000023.10:g.153296090C>A; NC_000023.10:g.153296090C>T
CLNSRC HGMD
CLNACC RCV000132951.2, RCV000081194.10, RCV000202529.1, RCV000224642.1,