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rs193922679

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs193922679(A;T)
Make rs193922679(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154031254
GeneMECP2
is asnp
is mentioned by
dbSNPrs193922679
ebirs193922679
HLIrs193922679
Exacrs193922679
Varsomers193922679
Maprs193922679
PheGenIrs193922679
hapmaprs193922679
1000 genomesrs193922679
hgdprs193922679
ensemblrs193922679
gopubmedrs193922679
geneviewrs193922679
scholarrs193922679
googlers193922679
pharmgkbrs193922679
gwascentralrs193922679
openSNPrs193922679
23andMers193922679
23andMe allrs193922679
SNP Nexus

SNPshotrs193922679
SNPdbers193922679
MSV3drs193922679
GWAS Ctlgrs193922679
Max Magnitude0
ClinVar
Risk rs193922679(T;T)
Alt rs193922679(T;T)
Reference rs193922679(A;A)
Significance Other
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296705T>A
CLNSRC ClinVar
CLNACC RCV000030165.3,