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rs386134191

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs386134191(C;G)
Make rs386134191(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position132370255
GeneMIR4750, SLC22A5
is asnp
is mentioned by
dbSNPrs386134191
ebirs386134191
HLIrs386134191
Exacrs386134191
Varsomers386134191
Maprs386134191
PheGenIrs386134191
hapmaprs386134191
1000 genomesrs386134191
hgdprs386134191
ensemblrs386134191
gopubmedrs386134191
geneviewrs386134191
scholarrs386134191
googlers386134191
pharmgkbrs386134191
gwascentralrs386134191
openSNPrs386134191
23andMers386134191
23andMe allrs386134191
SNP Nexus

SNPshotrs386134191
SNPdbers386134191
MSV3drs386134191
GWAS Ctlgrs386134191
Max Magnitude0
ClinVar
Risk rs386134191(G;G) rs386134191(T;T)
Alt rs386134191(G;G) rs386134191(T;T)
Reference Rs386134191(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.131705947C>G
CLNSRC ARUP SLC22A5
CLNACC RCV000022316.2,