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rs786204316

From SNPedia

Orientationminus
Geno Mag Summary
(CA;CA) 0 common in clinvar
Make rs786204316(-;-)
Make rs786204316(-;CA)
ReferenceGRCh38.p2 38.2/146
ChromosomeX
Position154030417
GeneMECP2
is asnp
is mentioned by
dbSNPrs786204316
ebirs786204316
HLIrs786204316
Exacrs786204316
Varsomers786204316
Maprs786204316
PheGenIrs786204316
hapmaprs786204316
1000 genomesrs786204316
hgdprs786204316
ensemblrs786204316
gopubmedrs786204316
geneviewrs786204316
scholarrs786204316
googlers786204316
pharmgkbrs786204316
gwascentralrs786204316
openSNPrs786204316
23andMers786204316
23andMe allrs786204316
SNP Nexus

SNPshotrs786204316
SNPdbers786204316
MSV3drs786204316
GWAS Ctlgrs786204316
Max Magnitude0
ClinVar
Risk rs786204316(;)
Alt rs786204316(;)
Reference rs786204316(CA;CA)
Significance Probable-Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153295868_153295869delTG
CLNSRC
CLNACC RCV000168708.1,