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rs786204307

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786204307(-;-)
Make rs786204307(-;C)
ReferenceGRCh38.p2 38.2/146
ChromosomeX
Position154031255
GeneMECP2
is asnp
is mentioned by
dbSNPrs786204307
ebirs786204307
HLIrs786204307
Exacrs786204307
Varsomers786204307
Maprs786204307
PheGenIrs786204307
hapmaprs786204307
1000 genomesrs786204307
hgdprs786204307
ensemblrs786204307
gopubmedrs786204307
geneviewrs786204307
scholarrs786204307
googlers786204307
pharmgkbrs786204307
gwascentralrs786204307
openSNPrs786204307
23andMers786204307
23andMe allrs786204307
SNP Nexus

SNPshotrs786204307
SNPdbers786204307
MSV3drs786204307
GWAS Ctlgrs786204307
Max Magnitude0
ClinVar
Risk rs786204307(;)
Alt rs786204307(;)
Reference rs786204307(C;C)
Significance Probable-Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296706delG
CLNSRC
CLNACC RCV000168684.1,