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rs796052033

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796052033(A;A)
Make rs796052033(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position132384263
GeneSLC22A5
is asnp
is mentioned by
dbSNPrs796052033
ebirs796052033
HLIrs796052033
Exacrs796052033
Varsomers796052033
Maprs796052033
PheGenIrs796052033
hapmaprs796052033
1000 genomesrs796052033
hgdprs796052033
ensemblrs796052033
gopubmedrs796052033
geneviewrs796052033
scholarrs796052033
googlers796052033
pharmgkbrs796052033
gwascentralrs796052033
openSNPrs796052033
23andMers796052033
23andMe allrs796052033
SNP Nexus

SNPshotrs796052033
SNPdbers796052033
MSV3drs796052033
GWAS Ctlgrs796052033
Max Magnitude0
ClinVar
Risk rs796052033(A;A)
Alt rs796052033(A;A)
Reference rs796052033(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SLC22A5
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.131719955T>A
CLNSRC
CLNACC RCV000186135.1,