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rs796053287

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796053287(C;C)
Make rs796053287(C;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position136040093
GeneSLC9A6
is asnp
is mentioned by
dbSNPrs796053287
ebirs796053287
HLIrs796053287
Exacrs796053287
Varsomers796053287
Maprs796053287
PheGenIrs796053287
hapmaprs796053287
1000 genomesrs796053287
hgdprs796053287
ensemblrs796053287
gopubmedrs796053287
geneviewrs796053287
scholarrs796053287
googlers796053287
pharmgkbrs796053287
gwascentralrs796053287
openSNPrs796053287
23andMers796053287
23andMe allrs796053287
SNP Nexus

SNPshotrs796053287
SNPdbers796053287
MSV3drs796053287
GWAS Ctlgrs796053287
Max Magnitude0
ClinVar
Risk rs796053287(C;C)
Alt rs796053287(C;C)
Reference rs796053287(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SLC9A6
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.135122252T>C
CLNSRC
CLNACC RCV000189414.2,