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rs386134199

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs386134199(C;T)
Make rs386134199(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position132384290
GeneSLC22A5
is asnp
is mentioned by
dbSNPrs386134199
ebirs386134199
HLIrs386134199
Exacrs386134199
Varsomers386134199
Maprs386134199
PheGenIrs386134199
hapmaprs386134199
1000 genomesrs386134199
hgdprs386134199
ensemblrs386134199
gopubmedrs386134199
geneviewrs386134199
scholarrs386134199
googlers386134199
pharmgkbrs386134199
gwascentralrs386134199
openSNPrs386134199
23andMers386134199
23andMe allrs386134199
SNP Nexus

SNPshotrs386134199
SNPdbers386134199
MSV3drs386134199
GWAS Ctlgrs386134199
Max Magnitude0
ClinVar
Risk rs386134199(T;T)
Alt rs386134199(T;T)
Reference rs386134199(C;C)
Significance Pathogenic
Disease Renal carnitine transport defect not provided
Variation info
Gene SLC22A5
CLNDBN Renal carnitine transport defect not provided
Reversed 0
HGVS NC_000005.9:g.131719982C>T
CLNSRC ARUP SLC22A5
CLNACC RCV000022332.2, RCV000186137.1,