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rs179363901

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs179363901(C;T)
Make rs179363901(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154097661
GeneMECP2
is asnp
is mentioned by
dbSNPrs179363901
ebirs179363901
HLIrs179363901
Exacrs179363901
Varsomers179363901
Maprs179363901
PheGenIrs179363901
hapmaprs179363901
1000 genomesrs179363901
hgdprs179363901
ensemblrs179363901
gopubmedrs179363901
geneviewrs179363901
scholarrs179363901
googlers179363901
pharmgkbrs179363901
gwascentralrs179363901
openSNPrs179363901
23andMers179363901
23andMe allrs179363901
SNP Nexus

SNPshotrs179363901
SNPdbers179363901
MSV3drs179363901
GWAS Ctlgrs179363901
Max Magnitude0
ClinVar
Risk rs179363901(T;T)
Alt rs179363901(T;T)
Reference rs179363901(C;C)
Significance Other
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153363118G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000012619.26,