Have questions? Visit https://www.reddit.com/r/SNPedia

rs145068530

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs145068530(A;G)
Make rs145068530(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position132384178
GeneSLC22A5
is asnp
is mentioned by
dbSNPrs145068530
dbSNP (classic)rs145068530
ClinGenrs145068530
ebirs145068530
HLIrs145068530
Exacrs145068530
Gnomadrs145068530
Varsomers145068530
LitVarrs145068530
Maprs145068530
PheGenIrs145068530
Biobankrs145068530
1000 genomesrs145068530
hgdprs145068530
ensemblrs145068530
geneviewrs145068530
scholarrs145068530
googlers145068530
pharmgkbrs145068530
gwascentralrs145068530
openSNPrs145068530
23andMers145068530
23andMe allrs145068530
SNPshotrs145068530
SNPdbers145068530
MSV3drs145068530
GWAS Ctlgrs145068530
Max Magnitude0
ClinVar
Risk rs145068530(G;G)
Alt rs145068530(G;G)
Reference Rs145068530(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SLC22A5
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.131719870A>G
CLNSRC
CLNACC RCV000434160.1,