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

rs386134201

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs386134201(A;C)
Make rs386134201(C;C)
ReferenceGRCh38 38.1/141
Chromosome5
Position132385326
GeneSLC22A5
is asnp
is mentioned by
dbSNPrs386134201
ebirs386134201
HLIrs386134201
Exacrs386134201
Varsomers386134201
Maprs386134201
PheGenIrs386134201
hapmaprs386134201
1000 genomesrs386134201
hgdprs386134201
ensemblrs386134201
gopubmedrs386134201
geneviewrs386134201
scholarrs386134201
googlers386134201
pharmgkbrs386134201
gwascentralrs386134201
openSNPrs386134201
23andMers386134201
23andMe allrs386134201
SNP Nexus

SNPshotrs386134201
SNPdbers386134201
MSV3drs386134201
GWAS Ctlgrs386134201
Max Magnitude0
ClinVar
Risk rs386134201(C;C)
Alt rs386134201(C;C)
Reference rs386134201(A;A)
Significance Untested
Disease Renal carnitine transport defect
Variation info
Gene SLC22A5
CLNDBN Renal carnitine transport defect
Reversed 0
HGVS NC_000005.9:g.131721018A>C
CLNSRC ARUP SLC22A5
CLNACC RCV000022337.2,