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

rs63749065

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GCCACGGCCGCAG;GCCACGGCCGCAG) 0 common in clinvar
Make rs63749065(-;-)
Make rs63749065(-;GCCACGGCCGCAG)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154030486
GeneMECP2
is asnp
is mentioned by
dbSNPrs63749065
ebirs63749065
HLIrs63749065
Exacrs63749065
Varsomers63749065
Maprs63749065
PheGenIrs63749065
hapmaprs63749065
1000 genomesrs63749065
hgdprs63749065
ensemblrs63749065
gopubmedrs63749065
geneviewrs63749065
scholarrs63749065
googlers63749065
pharmgkbrs63749065
gwascentralrs63749065
openSNPrs63749065
23andMers63749065
23andMe allrs63749065
SNP Nexus

SNPshotrs63749065
SNPdbers63749065
MSV3drs63749065
GWAS Ctlgrs63749065
Max Magnitude0
ClinVar
Risk rs63749065(;)
Alt rs63749065(;)
Reference rs63749065(GCCACGGCCGCAG;GCCACGGCCGCAG)
Significance Pathogenic
Disease not provided
Variation info
Gene MECP2
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.153295937_153295949delCTGCGGCCGTGGC
CLNSRC
CLNACC RCV000132992.2,