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rs61749708

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs61749708(-;-)
Make rs61749708(-;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154031262
GeneMECP2
is asnp
is mentioned by
dbSNPrs61749708
ebirs61749708
HLIrs61749708
Exacrs61749708
Varsomers61749708
Maprs61749708
PheGenIrs61749708
hapmaprs61749708
1000 genomesrs61749708
hgdprs61749708
ensemblrs61749708
gopubmedrs61749708
geneviewrs61749708
scholarrs61749708
googlers61749708
pharmgkbrs61749708
gwascentralrs61749708
openSNPrs61749708
23andMers61749708
23andMe allrs61749708
SNP Nexus

SNPshotrs61749708
SNPdbers61749708
MSV3drs61749708
GWAS Ctlgrs61749708
Max Magnitude0
ClinVar
Risk rs61749708(;)
Alt rs61749708(;)
Reference rs61749708(G;G)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153296713delC
CLNSRC
CLNACC RCV000133161.2,