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rs796052039

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052039(A;A)
Make rs796052039(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position132378403
GeneSLC22A5
is asnp
is mentioned by
dbSNPrs796052039
ebirs796052039
HLIrs796052039
Exacrs796052039
Varsomers796052039
Maprs796052039
PheGenIrs796052039
hapmaprs796052039
1000 genomesrs796052039
hgdprs796052039
ensemblrs796052039
gopubmedrs796052039
geneviewrs796052039
scholarrs796052039
googlers796052039
pharmgkbrs796052039
gwascentralrs796052039
openSNPrs796052039
23andMers796052039
23andMe allrs796052039
SNP Nexus

SNPshotrs796052039
SNPdbers796052039
MSV3drs796052039
GWAS Ctlgrs796052039
Max Magnitude0
ClinVar
Risk rs796052039(A;A)
Alt rs796052039(A;A)
Reference rs796052039(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SLC22A5
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.131714095G>A
CLNSRC
CLNACC RCV000186154.1,