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rs796053293

From SNPedia

Orientationplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs796053293(-;C)
Make rs796053293(C;C)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position135994806
GeneSLC9A6
is asnp
is mentioned by
dbSNPrs796053293
ClinGenrs796053293
ebirs796053293
HLIrs796053293
Exacrs796053293
Varsomers796053293
Maprs796053293
PheGenIrs796053293
hapmaprs796053293
1000 genomesrs796053293
hgdprs796053293
ensemblrs796053293
gopubmedrs796053293
geneviewrs796053293
scholarrs796053293
googlers796053293
pharmgkbrs796053293
gwascentralrs796053293
openSNPrs796053293
23andMers796053293
23andMe allrs796053293
SNP Nexus

SNPshotrs796053293
SNPdbers796053293
MSV3drs796053293
GWAS Ctlgrs796053293
Max Magnitude0
ClinVar
Risk rs796053293(C;C)
Alt rs796053293(C;C)
Reference Rs796053293(;)
Significance Pathogenic
Disease not provided
Variation info
Gene SLC9A6
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.135076965dupC
CLNSRC
CLNACC RCV000189420.1,