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rs267608598

From SNPedia

Orientationminus
Geno Mag Summary
(CC;CC) 0 common in clinvar
Make rs267608598(-;-)
Make rs267608598(-;CC)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154030665
GeneMECP2
is asnp
is mentioned by
dbSNPrs267608598
ebirs267608598
HLIrs267608598
Exacrs267608598
Varsomers267608598
Maprs267608598
PheGenIrs267608598
hapmaprs267608598
1000 genomesrs267608598
hgdprs267608598
ensemblrs267608598
gopubmedrs267608598
geneviewrs267608598
scholarrs267608598
googlers267608598
pharmgkbrs267608598
gwascentralrs267608598
openSNPrs267608598
23andMers267608598
23andMe allrs267608598
SNP Nexus

SNPshotrs267608598
SNPdbers267608598
MSV3drs267608598
GWAS Ctlgrs267608598
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs267608598(CC;CC)
Significance Pathogenic
Disease not provided
Variation info
Gene MECP2
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.153296116_153296117delGG
CLNSRC
CLNACC RCV000132920.2,