Have questions? Visit https://www.reddit.com/r/SNPedia

rs63749012

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GGGGAGTGTGGTGGCAG;GGGGAGTGTGGTGGCAG) 0 common in clinvar
Make rs63749012(-;-)
Make rs63749012(-;GGGGAGTGTGGTGGCAG)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154030996
GeneMECP2
is asnp
is mentioned by
dbSNPrs63749012
ebirs63749012
HLIrs63749012
Exacrs63749012
Varsomers63749012
Maprs63749012
PheGenIrs63749012
hapmaprs63749012
1000 genomesrs63749012
hgdprs63749012
ensemblrs63749012
gopubmedrs63749012
geneviewrs63749012
scholarrs63749012
googlers63749012
pharmgkbrs63749012
gwascentralrs63749012
openSNPrs63749012
23andMers63749012
23andMe allrs63749012
SNP Nexus

SNPshotrs63749012
SNPdbers63749012
MSV3drs63749012
GWAS Ctlgrs63749012
Max Magnitude0
ClinVar
Risk rs63749012(;)
Alt rs63749012(;)
Reference rs63749012(GGGGAGTGTGGTGGCAG;GGGGAGTGTGGTGGCAG)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296447_153296463del17
CLNSRC
CLNACC RCV000133247.2,