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rs786205021

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786205021(-;-)
Make rs786205021(-;T)
Make rs786205021(T;T)
ReferenceGRCh38.p2 38.2/146
ChromosomeX
Position154030647
GeneMECP2
is asnp
is mentioned by
dbSNPrs786205021
ebirs786205021
HLIrs786205021
Exacrs786205021
Varsomers786205021
Maprs786205021
PheGenIrs786205021
hapmaprs786205021
1000 genomesrs786205021
hgdprs786205021
ensemblrs786205021
gopubmedrs786205021
geneviewrs786205021
scholarrs786205021
googlers786205021
pharmgkbrs786205021
gwascentralrs786205021
openSNPrs786205021
23andMers786205021
23andMe allrs786205021
SNP Nexus

SNPshotrs786205021
SNPdbers786205021
MSV3drs786205021
GWAS Ctlgrs786205021
Max Magnitude0
ClinVar
Risk rs786205021(T;T)
Alt rs786205021(T;T)
Reference rs786205021(;)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296098_153296099insA
CLNSRC
CLNACC RCV000170153.1,