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

rs63260260

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs63260260(-;-)
Make rs63260260(-;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154031133
GeneMECP2
is asnp
is mentioned by
dbSNPrs63260260
ebirs63260260
HLIrs63260260
Exacrs63260260
Varsomers63260260
Maprs63260260
PheGenIrs63260260
hapmaprs63260260
1000 genomesrs63260260
hgdprs63260260
ensemblrs63260260
gopubmedrs63260260
geneviewrs63260260
scholarrs63260260
googlers63260260
pharmgkbrs63260260
gwascentralrs63260260
openSNPrs63260260
23andMers63260260
23andMe allrs63260260
SNP Nexus

SNPshotrs63260260
SNPdbers63260260
MSV3drs63260260
GWAS Ctlgrs63260260
Max Magnitude0
ClinVar
Risk rs63260260(;)
Alt rs63260260(;)
Reference rs63260260(G;G)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296584delC
CLNSRC
CLNACC RCV000133203.2,