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rs786205042

From SNPedia

Orientationminus
Geno Mag Summary
(GCGAGGAGGAG;GCGAGGAGGAG) 0 common in clinvar
Make rs786205042(-;-)
Make rs786205042(-;GCGAGGAGGAG)
ReferenceGRCh38.p2 38.2/146
ChromosomeX
Position154097609
GeneMECP2
is asnp
is mentioned by
dbSNPrs786205042
ebirs786205042
HLIrs786205042
Exacrs786205042
Varsomers786205042
Maprs786205042
PheGenIrs786205042
hapmaprs786205042
1000 genomesrs786205042
hgdprs786205042
ensemblrs786205042
gopubmedrs786205042
geneviewrs786205042
scholarrs786205042
googlers786205042
pharmgkbrs786205042
gwascentralrs786205042
openSNPrs786205042
23andMers786205042
23andMe allrs786205042
SNP Nexus

SNPshotrs786205042
SNPdbers786205042
MSV3drs786205042
GWAS Ctlgrs786205042
Max Magnitude0
ClinVar
Risk rs786205042(;)
Alt rs786205042(;)
Reference rs786205042(GCGAGGAGGAG;GCGAGGAGGAG)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153363066_153363076delCTCCTCCTCGC
CLNSRC
CLNACC RCV000170288.1,