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rs786205044

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786205044(-;-)
Make rs786205044(-;CGAGGAGG)
Make rs786205044(CGAGGAGG;CGAGGAGG)
ReferenceGRCh38.p2 38.2/146
ChromosomeX
Position154097610
GeneMECP2
is asnp
is mentioned by
dbSNPrs786205044
ebirs786205044
HLIrs786205044
Exacrs786205044
Varsomers786205044
Maprs786205044
PheGenIrs786205044
hapmaprs786205044
1000 genomesrs786205044
hgdprs786205044
ensemblrs786205044
gopubmedrs786205044
geneviewrs786205044
scholarrs786205044
googlers786205044
pharmgkbrs786205044
gwascentralrs786205044
openSNPrs786205044
23andMers786205044
23andMe allrs786205044
SNP Nexus

SNPshotrs786205044
SNPdbers786205044
MSV3drs786205044
GWAS Ctlgrs786205044
Max Magnitude0
ClinVar
Risk rs786205044(CGAGGAGG;CGAGGAGG)
Alt rs786205044(CGAGGAGG;CGAGGAGG)
Reference rs786205044(;)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153363068_153363075dupCCTCCTCG
CLNSRC
CLNACC RCV000170290.1,