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rs796053291

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs796053291(-;G)
Make rs796053291(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position135998856
GeneSLC9A6
is asnp
is mentioned by
dbSNPrs796053291
dbSNP (old)rs796053291
ClinGenrs796053291
ebirs796053291
HLIrs796053291
Exacrs796053291
Gnomadrs796053291
Varsomers796053291
Maprs796053291
PheGenIrs796053291
Biobankrs796053291
1000 genomesrs796053291
hgdprs796053291
ensemblrs796053291
gopubmedrs796053291
geneviewrs796053291
scholarrs796053291
googlers796053291
pharmgkbrs796053291
gwascentralrs796053291
openSNPrs796053291
23andMers796053291
23andMe allrs796053291
SNP Nexus

SNPshotrs796053291
SNPdbers796053291
MSV3drs796053291
GWAS Ctlgrs796053291
Max Magnitude0
ClinVar
Risk rs796053291(G;G)
Alt rs796053291(G;G)
Reference Rs796053291(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene SLC9A6
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.135081015dupG
CLNSRC
CLNACC RCV000189418.1,