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rs398122849

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GGTGCTGCT;GGTGCTGCT) 0 common in clinvar
Make rs398122849(-;-)
Make rs398122849(-;GGTGCTGCT)
ReferenceGRCh38 38.1/141
ChromosomeX
Position136010554
GeneSLC9A6
is asnp
is mentioned by
dbSNPrs398122849
ebirs398122849
HLIrs398122849
Exacrs398122849
Varsomers398122849
Maprs398122849
PheGenIrs398122849
hapmaprs398122849
1000 genomesrs398122849
hgdprs398122849
ensemblrs398122849
gopubmedrs398122849
geneviewrs398122849
scholarrs398122849
googlers398122849
pharmgkbrs398122849
gwascentralrs398122849
openSNPrs398122849
23andMers398122849
23andMe allrs398122849
SNP Nexus

SNPshotrs398122849
SNPdbers398122849
MSV3drs398122849
GWAS Ctlgrs398122849
Max Magnitude0
ClinVar
Risk rs398122849(;)
Alt rs398122849(;)
Reference rs398122849(GGTGCTGCT;GGTGCTGCT)
Significance Pathogenic
Disease Christianson syndrome
Variation info
Gene SLC9A6
CLNDBN Christianson syndrome
Reversed 0
HGVS NC_000023.10:g.135092713_135092721delGGTGCTGCT
CLNSRC OMIM Allelic Variant
CLNACC RCV000022841.22,