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rs386134192

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs386134192(A;G)
Make rs386134192(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position132370316
GeneMIR4750, SLC22A5
is asnp
is mentioned by
dbSNPrs386134192
ebirs386134192
HLIrs386134192
Exacrs386134192
Varsomers386134192
Maprs386134192
PheGenIrs386134192
hapmaprs386134192
1000 genomesrs386134192
hgdprs386134192
ensemblrs386134192
gopubmedrs386134192
geneviewrs386134192
scholarrs386134192
googlers386134192
pharmgkbrs386134192
gwascentralrs386134192
openSNPrs386134192
23andMers386134192
23andMe allrs386134192
SNP Nexus

SNPshotrs386134192
SNPdbers386134192
MSV3drs386134192
GWAS Ctlgrs386134192
Max Magnitude0
ClinVar
Risk rs386134192(G;G)
Alt rs386134192(G;G)
Reference rs386134192(A;A)
Significance Untested
Disease Renal carnitine transport defect
Variation info
Gene LOC553103 SLC22A5
CLNDBN Renal carnitine transport defect
Reversed 0
HGVS NC_000005.9:g.131706008A>G
CLNSRC ARUP SLC22A5
CLNACC RCV000022317.2,