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rs122461162

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs122461162(C;T)
Make rs122461162(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position136024365
GeneSLC9A6
is asnp
is mentioned by
dbSNPrs122461162
ebirs122461162
HLIrs122461162
Exacrs122461162
Varsomers122461162
Maprs122461162
PheGenIrs122461162
hapmaprs122461162
1000 genomesrs122461162
hgdprs122461162
ensemblrs122461162
gopubmedrs122461162
geneviewrs122461162
scholarrs122461162
googlers122461162
pharmgkbrs122461162
gwascentralrs122461162
openSNPrs122461162
23andMers122461162
23andMe allrs122461162
SNP Nexus

SNPshotrs122461162
SNPdbers122461162
MSV3drs122461162
GWAS Ctlgrs122461162
Max Magnitude0
OMIM300231
Desc
Variant0002
Relatedalso
ClinVar
Risk rs122461162(T;T)
Alt rs122461162(T;T)
Reference rs122461162(C;C)
Significance Pathogenic
Disease Christianson syndrome
Variation info
Gene SLC9A6
CLNDBN Christianson syndrome
Reversed 0
HGVS NC_000023.10:g.135106524C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000012232.14,