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rs587784398

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587784398(-;-)
Make rs587784398(-;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position135985685
GeneSLC9A6
is asnp
is mentioned by
dbSNPrs587784398
ebirs587784398
HLIrs587784398
Exacrs587784398
Varsomers587784398
Maprs587784398
PheGenIrs587784398
hapmaprs587784398
1000 genomesrs587784398
hgdprs587784398
ensemblrs587784398
gopubmedrs587784398
geneviewrs587784398
scholarrs587784398
googlers587784398
pharmgkbrs587784398
gwascentralrs587784398
openSNPrs587784398
23andMers587784398
23andMe allrs587784398
SNP Nexus

SNPshotrs587784398
SNPdbers587784398
MSV3drs587784398
GWAS Ctlgrs587784398
Max Magnitude0
ClinVar
Risk rs587784398(;)
Alt rs587784398(;)
Reference rs587784398(G;G)
Significance Pathogenic
Disease Christianson syndrome
Variation info
Gene SLC9A6
CLNDBN Christianson syndrome
Reversed 0
HGVS NC_000023.10:g.135067844delG
CLNSRC
CLNACC RCV000147540.1,