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rs796053297

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CA;CA) 0 common in clinvar
Make rs796053297(-;-)
Make rs796053297(-;CA)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position136010495
GeneSLC9A6
is asnp
is mentioned by
dbSNPrs796053297
dbSNP (old)rs796053297
ClinGenrs796053297
ebirs796053297
HLIrs796053297
Exacrs796053297
Gnomadrs796053297
Varsomers796053297
Maprs796053297
PheGenIrs796053297
Biobankrs796053297
1000 genomesrs796053297
hgdprs796053297
ensemblrs796053297
gopubmedrs796053297
geneviewrs796053297
scholarrs796053297
googlers796053297
pharmgkbrs796053297
gwascentralrs796053297
openSNPrs796053297
23andMers796053297
23andMe allrs796053297
SNP Nexus

SNPshotrs796053297
SNPdbers796053297
MSV3drs796053297
GWAS Ctlgrs796053297
Max Magnitude0
ClinVar
Risk rs796053297(-;-)
Alt rs796053297(-;-)
Reference Rs796053297(CA;CA)
Significance Pathogenic
Disease not provided
Variation info
Gene SLC9A6
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.135092654_135092655delCA
CLNSRC
CLNACC RCV000189424.2,