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rs398123003

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398123003(G;T)
Make rs398123003(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position136030154
GeneSLC9A6
is asnp
is mentioned by
dbSNPrs398123003
ebirs398123003
HLIrs398123003
Exacrs398123003
Varsomers398123003
Maprs398123003
PheGenIrs398123003
hapmaprs398123003
1000 genomesrs398123003
hgdprs398123003
ensemblrs398123003
gopubmedrs398123003
geneviewrs398123003
scholarrs398123003
googlers398123003
pharmgkbrs398123003
gwascentralrs398123003
openSNPrs398123003
23andMers398123003
23andMe allrs398123003
SNP Nexus

SNPshotrs398123003
SNPdbers398123003
MSV3drs398123003
GWAS Ctlgrs398123003
Max Magnitude0
ClinVar
Risk rs398123003(T;T)
Alt rs398123003(T;T)
Reference rs398123003(G;G)
Significance Pathogenic
Disease Christianson syndrome
Variation info
Gene SLC9A6
CLNDBN Christianson syndrome
Reversed 0
HGVS NC_000023.10:g.135112313G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000077787.3,