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rs796052036

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052036(A;A)
Make rs796052036(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position132370014
GeneLOC553103, SLC22A5
is asnp
is mentioned by
dbSNPrs796052036
ebirs796052036
HLIrs796052036
Exacrs796052036
Varsomers796052036
Maprs796052036
PheGenIrs796052036
hapmaprs796052036
1000 genomesrs796052036
hgdprs796052036
ensemblrs796052036
gopubmedrs796052036
geneviewrs796052036
scholarrs796052036
googlers796052036
pharmgkbrs796052036
gwascentralrs796052036
openSNPrs796052036
23andMers796052036
23andMe allrs796052036
SNP Nexus

SNPshotrs796052036
SNPdbers796052036
MSV3drs796052036
GWAS Ctlgrs796052036
Max Magnitude0
ClinVar
Risk rs796052036(A;A)
Alt rs796052036(A;A)
Reference rs796052036(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene LOC553103 SLC22A5
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.131705706G>A
CLNSRC
CLNACC RCV000186149.1,