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rs386134198

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs386134198(A;G)
Make rs386134198(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position132384278
GeneSLC22A5
is asnp
is mentioned by
dbSNPrs386134198
ebirs386134198
HLIrs386134198
Exacrs386134198
Varsomers386134198
Maprs386134198
PheGenIrs386134198
hapmaprs386134198
1000 genomesrs386134198
hgdprs386134198
ensemblrs386134198
gopubmedrs386134198
geneviewrs386134198
scholarrs386134198
googlers386134198
pharmgkbrs386134198
gwascentralrs386134198
openSNPrs386134198
23andMers386134198
23andMe allrs386134198
SNP Nexus

SNPshotrs386134198
SNPdbers386134198
MSV3drs386134198
GWAS Ctlgrs386134198
Max Magnitude0
ClinVar
Risk rs386134198(G;G)
Alt rs386134198(G;G)
Reference rs386134198(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.131719970A>G
CLNSRC ARUP SLC22A5
CLNACC RCV000022330.2,