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

rs730882188

From SNPedia

Orientationplus
Geno Mag Summary
(AT;AT) 0 common in clinvar
Make rs730882188(-;-)
Make rs730882188(-;AT)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position135998486
GeneSLC9A6
is asnp
is mentioned by
dbSNPrs730882188
ebirs730882188
HLIrs730882188
Exacrs730882188
Varsomers730882188
Maprs730882188
PheGenIrs730882188
hapmaprs730882188
1000 genomesrs730882188
hgdprs730882188
ensemblrs730882188
gopubmedrs730882188
geneviewrs730882188
scholarrs730882188
googlers730882188
pharmgkbrs730882188
gwascentralrs730882188
openSNPrs730882188
23andMers730882188
23andMe allrs730882188
SNP Nexus

SNPshotrs730882188
SNPdbers730882188
MSV3drs730882188
GWAS Ctlgrs730882188
Max Magnitude0
ClinVar
Risk rs730882188(;)
Alt rs730882188(;)
Reference rs730882188(AT;AT)
Significance Pathogenic
Disease Christianson syndrome
Variation info
Gene SLC9A6
CLNDBN Christianson syndrome
Reversed 0
HGVS NC_000023.10:g.135080645_135080646delAT
CLNSRC OMIM Allelic Variant
CLNACC RCV000012234.12,