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rs796053285

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796053285(A;A)
Make rs796053285(A;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position136013373
GeneSLC9A6
is asnp
is mentioned by
dbSNPrs796053285
ebirs796053285
HLIrs796053285
Exacrs796053285
Varsomers796053285
Maprs796053285
PheGenIrs796053285
hapmaprs796053285
1000 genomesrs796053285
hgdprs796053285
ensemblrs796053285
gopubmedrs796053285
geneviewrs796053285
scholarrs796053285
googlers796053285
pharmgkbrs796053285
gwascentralrs796053285
openSNPrs796053285
23andMers796053285
23andMe allrs796053285
SNP Nexus

SNPshotrs796053285
SNPdbers796053285
MSV3drs796053285
GWAS Ctlgrs796053285
Max Magnitude0
ClinVar
Risk rs796053285(A;A)
Alt rs796053285(A;A)
Reference rs796053285(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SLC9A6
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.135095532G>A
CLNSRC
CLNACC RCV000189411.2,