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rs386134190

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs386134190(C;G)
Make rs386134190(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position132370250
GeneMIR4750, SLC22A5
is asnp
is mentioned by
dbSNPrs386134190
ebirs386134190
HLIrs386134190
Exacrs386134190
Varsomers386134190
Maprs386134190
PheGenIrs386134190
hapmaprs386134190
1000 genomesrs386134190
hgdprs386134190
ensemblrs386134190
gopubmedrs386134190
geneviewrs386134190
scholarrs386134190
googlers386134190
pharmgkbrs386134190
gwascentralrs386134190
openSNPrs386134190
23andMers386134190
23andMe allrs386134190
SNP Nexus

SNPshotrs386134190
SNPdbers386134190
MSV3drs386134190
GWAS Ctlgrs386134190
Max Magnitude0
ClinVar
Risk rs386134190(G;G)
Alt rs386134190(G;G)
Reference rs386134190(C;C)
Significance Untested
Disease Renal carnitine transport defect
Variation info
Gene LOC553103 SLC22A5
CLNDBN Renal carnitine transport defect
Reversed 0
HGVS NC_000005.9:g.131705942C>G
CLNSRC ARUP SLC22A5
CLNACC RCV000022315.2,