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rs63749009

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GCTTCTGCCT;GCTTCTGCCT) 0 common in clinvar
Make rs63749009(-;-)
Make rs63749009(-;GCTTCTGCCT)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154032346
GeneMECP2
is asnp
is mentioned by
dbSNPrs63749009
ebirs63749009
HLIrs63749009
Exacrs63749009
Varsomers63749009
Maprs63749009
PheGenIrs63749009
hapmaprs63749009
1000 genomesrs63749009
hgdprs63749009
ensemblrs63749009
gopubmedrs63749009
geneviewrs63749009
scholarrs63749009
googlers63749009
pharmgkbrs63749009
gwascentralrs63749009
openSNPrs63749009
23andMers63749009
23andMe allrs63749009
SNP Nexus

SNPshotrs63749009
SNPdbers63749009
MSV3drs63749009
GWAS Ctlgrs63749009
Max Magnitude0
ClinVar
Risk rs63749009(;)
Alt rs63749009(;)
Reference rs63749009(GCTTCTGCCT;GCTTCTGCCT)
Significance Pathogenic
Disease not provided
Variation info
Gene MECP2
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.153297797_153297806delAGGCAGAAGC
CLNSRC
CLNACC RCV000133037.2,