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rs786205892

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786205892(A;T)
Make rs786205892(T;T)
ReferenceGRCh38.p2 38.2/146
ChromosomeX
Position154092209
GeneMECP2
is asnp
is mentioned by
dbSNPrs786205892
ebirs786205892
HLIrs786205892
Exacrs786205892
Varsomers786205892
Maprs786205892
PheGenIrs786205892
hapmaprs786205892
1000 genomesrs786205892
hgdprs786205892
ensemblrs786205892
gopubmedrs786205892
geneviewrs786205892
scholarrs786205892
googlers786205892
pharmgkbrs786205892
gwascentralrs786205892
openSNPrs786205892
23andMers786205892
23andMe allrs786205892
SNP Nexus

SNPshotrs786205892
SNPdbers786205892
MSV3drs786205892
GWAS Ctlgrs786205892
Max Magnitude0
ClinVar
Risk rs786205892(T;T)
Alt rs786205892(T;T)
Reference rs786205892(A;A)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153357667T>A
CLNSRC
CLNACC RCV000172861.1,