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

rs63094662

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0
(G;G) 0 common in clinvar
Make rs63094662(A;A)
Make rs63094662(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154030648
GeneMECP2
is asnp
is mentioned by
dbSNPrs63094662
ClinGenrs63094662
ebirs63094662
HLIrs63094662
Exacrs63094662
Varsomers63094662
Maprs63094662
PheGenIrs63094662
hapmaprs63094662
1000 genomesrs63094662
hgdprs63094662
ensemblrs63094662
gopubmedrs63094662
geneviewrs63094662
scholarrs63094662
googlers63094662
pharmgkbrs63094662
gwascentralrs63094662
openSNPrs63094662
23andMers63094662
23andMe allrs63094662
SNP Nexus

SNPshotrs63094662
SNPdbers63094662
MSV3drs63094662
GWAS Ctlgrs63094662
Max Magnitude0
ClinVar
Risk rs63094662(A;A) rs63094662(T;T)
Alt rs63094662(A;A) rs63094662(T;T)
Reference Rs63094662(G;G)
Significance Pathogenic
Disease Mental retardation Rett syndrome not specified
Variation info
Gene MECP2
CLNDBN Mental retardation, X-linked, syndromic 13 Rett syndrome not specified
Reversed 1
HGVS NC_000023.10:g.153296099C>A; NC_000023.10:g.153296099C>T
CLNSRC OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000012588.22, RCV000146349.1, RCV000132947.2,