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rs1057519216

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057519216(G;T)
Make rs1057519216(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position154030582
GeneMECP2
is asnp
is mentioned by
dbSNPrs1057519216
dbSNP (old)rs1057519216
ClinGenrs1057519216
ebirs1057519216
HLIrs1057519216
Exacrs1057519216
Gnomadrs1057519216
Varsomers1057519216
Maprs1057519216
PheGenIrs1057519216
Biobankrs1057519216
1000 genomesrs1057519216
hgdprs1057519216
ensemblrs1057519216
gopubmedrs1057519216
geneviewrs1057519216
scholarrs1057519216
googlers1057519216
pharmgkbrs1057519216
gwascentralrs1057519216
openSNPrs1057519216
23andMers1057519216
23andMe allrs1057519216
SNPshotrs1057519216
SNPdbers1057519216
MSV3drs1057519216
GWAS Ctlgrs1057519216
Max Magnitude0
ClinVar
Risk rs1057519216(T;T)
Alt rs1057519216(T;T)
Reference Rs1057519216(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MECP2
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.153296033C>A
CLNSRC
CLNACC RCV000415905.1,