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rs796053283

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796053283(A;A)
Make rs796053283(A;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position136033494
GeneSLC9A6
is asnp
is mentioned by
dbSNPrs796053283
ebirs796053283
HLIrs796053283
Exacrs796053283
Varsomers796053283
Maprs796053283
PheGenIrs796053283
hapmaprs796053283
1000 genomesrs796053283
hgdprs796053283
ensemblrs796053283
gopubmedrs796053283
geneviewrs796053283
scholarrs796053283
googlers796053283
pharmgkbrs796053283
gwascentralrs796053283
openSNPrs796053283
23andMers796053283
23andMe allrs796053283
SNP Nexus

SNPshotrs796053283
SNPdbers796053283
MSV3drs796053283
GWAS Ctlgrs796053283
Max Magnitude0
ClinVar
Risk rs796053283(A;A)
Alt rs796053283(A;A)
Reference rs796053283(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SLC9A6
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.135115653G>A
CLNSRC
CLNACC RCV000189409.1,