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rs267608644

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267608644(G;T)
Make rs267608644(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position18604632
GeneCDKL5
is asnp
is mentioned by
dbSNPrs267608644
ebirs267608644
HLIrs267608644
Exacrs267608644
Varsomers267608644
Maprs267608644
PheGenIrs267608644
hapmaprs267608644
1000 genomesrs267608644
hgdprs267608644
ensemblrs267608644
gopubmedrs267608644
geneviewrs267608644
scholarrs267608644
googlers267608644
pharmgkbrs267608644
gwascentralrs267608644
openSNPrs267608644
23andMers267608644
23andMe allrs267608644
SNP Nexus

SNPshotrs267608644
SNPdbers267608644
MSV3drs267608644
GWAS Ctlgrs267608644
Max Magnitude0
ClinVar
Risk rs267608644(T;T)
Alt rs267608644(T;T)
Reference rs267608644(G;G)
Significance Pathogenic
Disease Atypical Rett syndrome
Variation info
Gene CDKL5
CLNDBN Atypical Rett syndrome
Reversed 0
HGVS NC_000023.10:g.18622752G>T
CLNSRC RettBASE (CDKL5)
CLNACC RCV000133329.2,