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rs786204309

From SNPedia

Orientationminus
Geno Mag Summary
(TGAGGGGGGTGGGGC;TGAGGGGGGTGGGGC) 0 common in clinvar
Make rs786204309(-;-)
Make rs786204309(-;TGAGGGGGGTGGGGC)
ReferenceGRCh38.p2 38.2/146
ChromosomeX
Position154031112
GeneMECP2
is asnp
is mentioned by
dbSNPrs786204309
ebirs786204309
HLIrs786204309
Exacrs786204309
Varsomers786204309
Maprs786204309
PheGenIrs786204309
hapmaprs786204309
1000 genomesrs786204309
hgdprs786204309
ensemblrs786204309
gopubmedrs786204309
geneviewrs786204309
scholarrs786204309
googlers786204309
pharmgkbrs786204309
gwascentralrs786204309
openSNPrs786204309
23andMers786204309
23andMe allrs786204309
SNP Nexus

SNPshotrs786204309
SNPdbers786204309
MSV3drs786204309
GWAS Ctlgrs786204309
Max Magnitude0
ClinVar
Risk rs786204309(;)
Alt rs786204309(;)
Reference rs786204309(TGAGGGGGGTGGGGC;TGAGGGGGGTGGGGC)
Significance Probable-Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296563_153296577delGCCCCACCCCCCTCA
CLNSRC
CLNACC RCV000168688.1,