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

rs386134193

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs386134193(A;A)
Make rs386134193(A;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position132378435
GeneSLC22A5
is asnp
is mentioned by
dbSNPrs386134193
ebirs386134193
HLIrs386134193
Exacrs386134193
Varsomers386134193
Maprs386134193
PheGenIrs386134193
hapmaprs386134193
1000 genomesrs386134193
hgdprs386134193
ensemblrs386134193
gopubmedrs386134193
geneviewrs386134193
scholarrs386134193
googlers386134193
pharmgkbrs386134193
gwascentralrs386134193
openSNPrs386134193
23andMers386134193
23andMe allrs386134193
SNP Nexus

SNPshotrs386134193
SNPdbers386134193
MSV3drs386134193
GWAS Ctlgrs386134193
Max Magnitude0
ClinVar
Risk rs386134193(A,C,T;A,C,T)
Alt rs386134193(A,C,T;A,C,T)
Reference rs386134193(G;G)
Significance Untested
Disease Renal carnitine transport defect
Variation info
Gene SLC22A5
CLNDBN Renal carnitine transport defect
Reversed 0
HGVS NC_000005.9:g.131714127G>A
CLNSRC ClinVar
CLNACC RCV000022322.2,