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rs61749744

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs61749744(-;-)
Make rs61749744(-;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154031113
GeneMECP2
is asnp
is mentioned by
dbSNPrs61749744
ebirs61749744
HLIrs61749744
Exacrs61749744
Varsomers61749744
Maprs61749744
PheGenIrs61749744
hapmaprs61749744
1000 genomesrs61749744
hgdprs61749744
ensemblrs61749744
gopubmedrs61749744
geneviewrs61749744
scholarrs61749744
googlers61749744
pharmgkbrs61749744
gwascentralrs61749744
openSNPrs61749744
23andMers61749744
23andMe allrs61749744
SNP Nexus

SNPshotrs61749744
SNPdbers61749744
MSV3drs61749744
GWAS Ctlgrs61749744
Max Magnitude0
ClinVar
Risk rs61749744(;)
Alt rs61749744(;)
Reference rs61749744(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene MECP2
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.153296564delC
CLNSRC
CLNACC RCV000133209.2,