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rs796052038

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796052038(C;C)
Make rs796052038(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position132378402
GeneSLC22A5
is asnp
is mentioned by
dbSNPrs796052038
ebirs796052038
HLIrs796052038
Exacrs796052038
Varsomers796052038
Maprs796052038
PheGenIrs796052038
hapmaprs796052038
1000 genomesrs796052038
hgdprs796052038
ensemblrs796052038
gopubmedrs796052038
geneviewrs796052038
scholarrs796052038
googlers796052038
pharmgkbrs796052038
gwascentralrs796052038
openSNPrs796052038
23andMers796052038
23andMe allrs796052038
SNP Nexus

SNPshotrs796052038
SNPdbers796052038
MSV3drs796052038
GWAS Ctlgrs796052038
Max Magnitude0
ClinVar
Risk rs796052038(C;C)
Alt rs796052038(C;C)
Reference rs796052038(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SLC22A5
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.131714094T>C
CLNSRC
CLNACC RCV000186153.1,