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rs796053282

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796053282(A;A)
Make rs796053282(A;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position135998559
GeneSLC9A6
is asnp
is mentioned by
dbSNPrs796053282
ebirs796053282
HLIrs796053282
Exacrs796053282
Varsomers796053282
Maprs796053282
PheGenIrs796053282
hapmaprs796053282
1000 genomesrs796053282
hgdprs796053282
ensemblrs796053282
gopubmedrs796053282
geneviewrs796053282
scholarrs796053282
googlers796053282
pharmgkbrs796053282
gwascentralrs796053282
openSNPrs796053282
23andMers796053282
23andMe allrs796053282
SNP Nexus

SNPshotrs796053282
SNPdbers796053282
MSV3drs796053282
GWAS Ctlgrs796053282
Max Magnitude0
ClinVar
Risk rs796053282(A;A)
Alt rs796053282(A;A)
Reference rs796053282(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SLC9A6
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.135080718G>A
CLNSRC
CLNACC RCV000189408.1,