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rs786205022

From SNPedia

Orientationminus
Geno Mag Summary
(CGCAGA;CGCAGA) 0 common in clinvar
Make rs786205022(-;-)
Make rs786205022(-;CGCAGA)
ReferenceGRCh38.p2 38.2/146
ChromosomeX
Position154030485
GeneMECP2
is asnp
is mentioned by
dbSNPrs786205022
ebirs786205022
HLIrs786205022
Exacrs786205022
Varsomers786205022
Maprs786205022
PheGenIrs786205022
hapmaprs786205022
1000 genomesrs786205022
hgdprs786205022
ensemblrs786205022
gopubmedrs786205022
geneviewrs786205022
scholarrs786205022
googlers786205022
pharmgkbrs786205022
gwascentralrs786205022
openSNPrs786205022
23andMers786205022
23andMe allrs786205022
SNP Nexus

SNPshotrs786205022
SNPdbers786205022
MSV3drs786205022
GWAS Ctlgrs786205022
Max Magnitude0
ClinVar
Risk rs786205022(;)
Alt rs786205022(;)
Reference rs786205022(CGCAGA;CGCAGA)
Significance Pathogenic
Disease not provided
Variation info
Gene MECP2
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.153295936_153295941delTCTGCG
CLNSRC
CLNACC RCV000170158.1,