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rs786205038

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786205038(-;-)
Make rs786205038(-;CGCCG)
Make rs786205038(CGCCG;CGCCG)
ReferenceGRCh38.p2 38.2/146
ChromosomeX
Position154097638
GeneMECP2
is asnp
is mentioned by
dbSNPrs786205038
ebirs786205038
HLIrs786205038
Exacrs786205038
Varsomers786205038
Maprs786205038
PheGenIrs786205038
hapmaprs786205038
1000 genomesrs786205038
hgdprs786205038
ensemblrs786205038
gopubmedrs786205038
geneviewrs786205038
scholarrs786205038
googlers786205038
pharmgkbrs786205038
gwascentralrs786205038
openSNPrs786205038
23andMers786205038
23andMe allrs786205038
SNP Nexus

SNPshotrs786205038
SNPdbers786205038
MSV3drs786205038
GWAS Ctlgrs786205038
Max Magnitude0
ClinVar
Risk rs786205038(CGCCG;CGCCG)
Alt rs786205038(CGCCG;CGCCG)
Reference rs786205038(;)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153363096_153363100dupCGGCG
CLNSRC
CLNACC RCV000170282.1,