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rs786205895

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786205895(-;-)
Make rs786205895(-;A)
ReferenceGRCh38.p2 38.2/146
ChromosomeX
Position154031438
GeneMECP2
is asnp
is mentioned by
dbSNPrs786205895
ClinGenrs786205895
ebirs786205895
HLIrs786205895
Exacrs786205895
Varsomers786205895
Maprs786205895
PheGenIrs786205895
hapmaprs786205895
1000 genomesrs786205895
hgdprs786205895
ensemblrs786205895
gopubmedrs786205895
geneviewrs786205895
scholarrs786205895
googlers786205895
pharmgkbrs786205895
gwascentralrs786205895
openSNPrs786205895
23andMers786205895
23andMe allrs786205895
SNP Nexus

SNPshotrs786205895
SNPdbers786205895
MSV3drs786205895
GWAS Ctlgrs786205895
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs786205895(A;A)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296889delT
CLNSRC
CLNACC RCV000172870.1,