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rs61748394

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs61748394(-;-)
Make rs61748394(-;A)
Make rs61748394(A;A)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154031405
GeneMECP2
is asnp
is mentioned by
dbSNPrs61748394
ebirs61748394
HLIrs61748394
Exacrs61748394
Varsomers61748394
Maprs61748394
PheGenIrs61748394
hapmaprs61748394
1000 genomesrs61748394
hgdprs61748394
ensemblrs61748394
gopubmedrs61748394
geneviewrs61748394
scholarrs61748394
googlers61748394
pharmgkbrs61748394
gwascentralrs61748394
openSNPrs61748394
23andMers61748394
23andMe allrs61748394
SNP Nexus

SNPshotrs61748394
SNPdbers61748394
MSV3drs61748394
GWAS Ctlgrs61748394
Max Magnitude0
ClinVar
Risk rs61748394(A;A)
Alt rs61748394(A;A)
Reference rs61748394(;)
Significance Pathogenic
Disease not provided
Variation info
Gene MECP2
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.153296857dupT
CLNSRC
CLNACC RCV000133105.2,