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rs796053296

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796053296(C;G)
Make rs796053296(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position135985722
GeneSLC9A6
is asnp
is mentioned by
dbSNPrs796053296
ebirs796053296
HLIrs796053296
Exacrs796053296
Varsomers796053296
Maprs796053296
PheGenIrs796053296
hapmaprs796053296
1000 genomesrs796053296
hgdprs796053296
ensemblrs796053296
gopubmedrs796053296
geneviewrs796053296
scholarrs796053296
googlers796053296
pharmgkbrs796053296
gwascentralrs796053296
openSNPrs796053296
23andMers796053296
23andMe allrs796053296
SNP Nexus

SNPshotrs796053296
SNPdbers796053296
MSV3drs796053296
GWAS Ctlgrs796053296
Max Magnitude0
ClinVar
Risk rs796053296(G;G)
Alt rs796053296(G;G)
Reference rs796053296(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SLC9A6
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.135067881C>G
CLNSRC
CLNACC RCV000189423.1,