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rs786205025

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786205025(-;-)
Make rs786205025(-;GAAG)
Make rs786205025(GAAG;GAAG)
ReferenceGRCh38.p2 38.2/146
ChromosomeX
Position154032262
GeneMECP2
is asnp
is mentioned by
dbSNPrs786205025
ebirs786205025
HLIrs786205025
Exacrs786205025
Varsomers786205025
Maprs786205025
PheGenIrs786205025
hapmaprs786205025
1000 genomesrs786205025
hgdprs786205025
ensemblrs786205025
gopubmedrs786205025
geneviewrs786205025
scholarrs786205025
googlers786205025
pharmgkbrs786205025
gwascentralrs786205025
openSNPrs786205025
23andMers786205025
23andMe allrs786205025
SNP Nexus

SNPshotrs786205025
SNPdbers786205025
MSV3drs786205025
GWAS Ctlgrs786205025
Max Magnitude0
ClinVar
Risk rs786205025(GAAG;GAAG)
Alt rs786205025(GAAG;GAAG)
Reference rs786205025(;)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153297714_153297717dupCTTC
CLNSRC
CLNACC RCV000170189.1,