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rs796053284

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796053284(A;A)
Make rs796053284(A;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position135998563
GeneSLC9A6
is asnp
is mentioned by
dbSNPrs796053284
ebirs796053284
HLIrs796053284
Exacrs796053284
Varsomers796053284
Maprs796053284
PheGenIrs796053284
hapmaprs796053284
1000 genomesrs796053284
hgdprs796053284
ensemblrs796053284
gopubmedrs796053284
geneviewrs796053284
scholarrs796053284
googlers796053284
pharmgkbrs796053284
gwascentralrs796053284
openSNPrs796053284
23andMers796053284
23andMe allrs796053284
SNP Nexus

SNPshotrs796053284
SNPdbers796053284
MSV3drs796053284
GWAS Ctlgrs796053284
Max Magnitude0
ClinVar
Risk rs796053284(A;A)
Alt rs796053284(A;A)
Reference rs796053284(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SLC9A6
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.135080722G>A
CLNSRC
CLNACC RCV000189410.1,