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rs386134226

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs386134226(G;T)
Make rs386134226(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position132393812
GeneSLC22A5
is asnp
is mentioned by
dbSNPrs386134226
ebirs386134226
HLIrs386134226
Exacrs386134226
Varsomers386134226
Maprs386134226
PheGenIrs386134226
hapmaprs386134226
1000 genomesrs386134226
hgdprs386134226
ensemblrs386134226
gopubmedrs386134226
geneviewrs386134226
scholarrs386134226
googlers386134226
pharmgkbrs386134226
gwascentralrs386134226
openSNPrs386134226
23andMers386134226
23andMe allrs386134226
SNP Nexus

SNPshotrs386134226
SNPdbers386134226
MSV3drs386134226
GWAS Ctlgrs386134226
Max Magnitude0
ClinVar
Risk rs386134226(T;T)
Alt rs386134226(T;T)
Reference rs386134226(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.131729504G>T
CLNSRC ARUP SLC22A5
CLNACC RCV000022388.2,