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rs797044508

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797044508(A;A)
Make rs797044508(A;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position135998481
GeneSLC9A6
is asnp
is mentioned by
dbSNPrs797044508
ebirs797044508
HLIrs797044508
Exacrs797044508
Varsomers797044508
Maprs797044508
PheGenIrs797044508
hapmaprs797044508
1000 genomesrs797044508
hgdprs797044508
ensemblrs797044508
gopubmedrs797044508
geneviewrs797044508
scholarrs797044508
googlers797044508
pharmgkbrs797044508
gwascentralrs797044508
openSNPrs797044508
23andMers797044508
23andMe allrs797044508
SNP Nexus

SNPshotrs797044508
SNPdbers797044508
MSV3drs797044508
GWAS Ctlgrs797044508
Max Magnitude0
ClinVar
Risk rs797044508(A;A)
Alt rs797044508(A;A)
Reference rs797044508(G;G)
Significance Pathogenic
Disease Christianson syndrome
Variation info
Gene SLC9A6
CLNDBN Christianson syndrome
Reversed 0
HGVS NC_000023.10:g.135080640G>A
CLNSRC
CLNACC RCV000153971.3,