Have questions? Visit https://www.reddit.com/r/SNPedia

rs267608505

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267608505(G;T)
Make rs267608505(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position18588006
GeneCDKL5
is asnp
is mentioned by
dbSNPrs267608505
ebirs267608505
HLIrs267608505
Exacrs267608505
Varsomers267608505
Maprs267608505
PheGenIrs267608505
hapmaprs267608505
1000 genomesrs267608505
hgdprs267608505
ensemblrs267608505
gopubmedrs267608505
geneviewrs267608505
scholarrs267608505
googlers267608505
pharmgkbrs267608505
gwascentralrs267608505
openSNPrs267608505
23andMers267608505
23andMe allrs267608505
SNP Nexus

SNPshotrs267608505
SNPdbers267608505
MSV3drs267608505
GWAS Ctlgrs267608505
Max Magnitude0
ClinVar
Risk rs267608505(T;T)
Alt rs267608505(T;T)
Reference rs267608505(G;G)
Significance Pathogenic
Disease Atypical Rett syndrome
Variation info
Gene CDKL5
CLNDBN Atypical Rett syndrome
Reversed 0
HGVS NC_000023.10:g.18606126G>T
CLNSRC RettBASE (CDKL5)
CLNACC RCV000133380.2,