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

rs587783095

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587783095(-;-)
Make rs587783095(-;C)
Make rs587783095(C;C)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154030537
GeneMECP2
is asnp
is mentioned by
dbSNPrs587783095
ebirs587783095
HLIrs587783095
Exacrs587783095
Varsomers587783095
Maprs587783095
PheGenIrs587783095
hapmaprs587783095
1000 genomesrs587783095
hgdprs587783095
ensemblrs587783095
gopubmedrs587783095
geneviewrs587783095
scholarrs587783095
googlers587783095
pharmgkbrs587783095
gwascentralrs587783095
openSNPrs587783095
23andMers587783095
23andMe allrs587783095
SNP Nexus

SNPshotrs587783095
SNPdbers587783095
MSV3drs587783095
GWAS Ctlgrs587783095
Max Magnitude0
ClinVar
Risk rs587783095(C;C)
Alt rs587783095(C;C)
Reference rs587783095(;)
Significance Pathogenic
Disease not provided
Variation info
Gene MECP2
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.153295989dupG
CLNSRC
CLNACC RCV000144761.1,