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

rs1057518568

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518568(-;-)
Make rs1057518568(-;C)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position154031013
GeneMECP2
is asnp
is mentioned by
dbSNPrs1057518568
dbSNP (old)rs1057518568
ClinGenrs1057518568
ebirs1057518568
HLIrs1057518568
Exacrs1057518568
Gnomadrs1057518568
Varsomers1057518568
LitVarrs1057518568
Maprs1057518568
PheGenIrs1057518568
Biobankrs1057518568
1000 genomesrs1057518568
hgdprs1057518568
ensemblrs1057518568
gopubmedrs1057518568
geneviewrs1057518568
scholarrs1057518568
googlers1057518568
pharmgkbrs1057518568
gwascentralrs1057518568
openSNPrs1057518568
23andMers1057518568
23andMe allrs1057518568
SNPshotrs1057518568
SNPdbers1057518568
MSV3drs1057518568
GWAS Ctlgrs1057518568
Max Magnitude0
ClinVar
Risk rs1057518568(-;-)
Alt rs1057518568(-;-)
Reference Rs1057518568(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MECP2
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.153296464delG
CLNSRC
CLNACC RCV000413774.1,