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rs796052035

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052035(A;A)
Make rs796052035(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position132392586
GeneSLC22A5
is asnp
is mentioned by
dbSNPrs796052035
ebirs796052035
HLIrs796052035
Exacrs796052035
Varsomers796052035
Maprs796052035
PheGenIrs796052035
hapmaprs796052035
1000 genomesrs796052035
hgdprs796052035
ensemblrs796052035
gopubmedrs796052035
geneviewrs796052035
scholarrs796052035
googlers796052035
pharmgkbrs796052035
gwascentralrs796052035
openSNPrs796052035
23andMers796052035
23andMe allrs796052035
SNP Nexus

SNPshotrs796052035
SNPdbers796052035
MSV3drs796052035
GWAS Ctlgrs796052035
Max Magnitude0
ClinVar
Risk rs796052035(A;A)
Alt rs796052035(A;A)
Reference rs796052035(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SLC22A5
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.131728278G>A
CLNSRC
CLNACC RCV000186145.1,