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rs63749010

From SNPedia

Orientationminus
Geno Mag Summary
(GGACACGGAAGCT;GGACACGGAAGCT) 0 common in clinvar
Make rs63749010(-;-)
Make rs63749010(-;GGACACGGAAGCT)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154032261
GeneMECP2
is asnp
is mentioned by
dbSNPrs63749010
ebirs63749010
HLIrs63749010
Exacrs63749010
Varsomers63749010
Maprs63749010
PheGenIrs63749010
hapmaprs63749010
1000 genomesrs63749010
hgdprs63749010
ensemblrs63749010
gopubmedrs63749010
geneviewrs63749010
scholarrs63749010
googlers63749010
pharmgkbrs63749010
gwascentralrs63749010
openSNPrs63749010
23andMers63749010
23andMe allrs63749010
SNP Nexus

SNPshotrs63749010
SNPdbers63749010
MSV3drs63749010
GWAS Ctlgrs63749010
Max Magnitude0
ClinVar
Risk rs63749010(;)
Alt rs63749010(;)
Reference rs63749010(GGACACGGAAGCT;GGACACGGAAGCT)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153297712_153297724delAGCTTCCGTGTCC
CLNSRC
CLNACC RCV000133063.2,