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rs587784399

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587784399(G;G)
Make rs587784399(G;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position136044696
GeneSLC9A6
is asnp
is mentioned by
dbSNPrs587784399
ebirs587784399
HLIrs587784399
Exacrs587784399
Varsomers587784399
Maprs587784399
PheGenIrs587784399
hapmaprs587784399
1000 genomesrs587784399
hgdprs587784399
ensemblrs587784399
gopubmedrs587784399
geneviewrs587784399
scholarrs587784399
googlers587784399
pharmgkbrs587784399
gwascentralrs587784399
openSNPrs587784399
23andMers587784399
23andMe allrs587784399
SNP Nexus

SNPshotrs587784399
SNPdbers587784399
MSV3drs587784399
GWAS Ctlgrs587784399
Max Magnitude0
ClinVar
Risk rs587784399(G;G)
Alt rs587784399(G;G)
Reference rs587784399(T;T)
Significance Pathogenic
Disease Christianson syndrome
Variation info
Gene SLC9A6
CLNDBN Christianson syndrome
Reversed 0
HGVS NC_000023.10:g.135126855T>G
CLNSRC
CLNACC RCV000147541.1,