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

rs1057522038

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057522038(A;G)
Make rs1057522038(G;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position154030921
GeneMECP2
is asnp
is mentioned by
dbSNPrs1057522038
dbSNP (old)rs1057522038
ClinGenrs1057522038
ebirs1057522038
HLIrs1057522038
Exacrs1057522038
Gnomadrs1057522038
Varsomers1057522038
Maprs1057522038
PheGenIrs1057522038
Biobankrs1057522038
1000 genomesrs1057522038
hgdprs1057522038
ensemblrs1057522038
gopubmedrs1057522038
geneviewrs1057522038
scholarrs1057522038
googlers1057522038
pharmgkbrs1057522038
gwascentralrs1057522038
openSNPrs1057522038
23andMers1057522038
23andMe allrs1057522038
SNPshotrs1057522038
SNPdbers1057522038
MSV3drs1057522038
GWAS Ctlgrs1057522038
Max Magnitude0
ClinVar
Risk rs1057522038(G;G)
Alt rs1057522038(G;G)
Reference Rs1057522038(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MECP2
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.153296372T>C
CLNSRC
CLNACC RCV000438431.1,