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

rs587783137

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587783137(C;T)
Make rs587783137(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154031260
GeneMECP2
is asnp
is mentioned by
dbSNPrs587783137
ebirs587783137
HLIrs587783137
Exacrs587783137
Varsomers587783137
Maprs587783137
PheGenIrs587783137
hapmaprs587783137
1000 genomesrs587783137
hgdprs587783137
ensemblrs587783137
gopubmedrs587783137
geneviewrs587783137
scholarrs587783137
googlers587783137
pharmgkbrs587783137
gwascentralrs587783137
openSNPrs587783137
23andMers587783137
23andMe allrs587783137
SNP Nexus

SNPshotrs587783137
SNPdbers587783137
MSV3drs587783137
GWAS Ctlgrs587783137
Max Magnitude0
ClinVar
Risk rs587783137(T;T)
Alt rs587783137(T;T)
Reference rs587783137(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MECP2
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.153296711G>A
CLNSRC
CLNACC RCV000144810.2,