Have questions? Visit https://www.reddit.com/r/SNPedia

rs386134189

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs386134189(-;-)
Make rs386134189(-;GGCTCGCCACC)
Make rs386134189(GGCTCGCCACC;GGCTCGCCACC)
ReferenceGRCh38 38.1/141
Chromosome5
Position132370237
GeneMIR4750, SLC22A5
is asnp
is mentioned by
dbSNPrs386134189
ebirs386134189
HLIrs386134189
Exacrs386134189
Varsomers386134189
Maprs386134189
PheGenIrs386134189
hapmaprs386134189
1000 genomesrs386134189
hgdprs386134189
ensemblrs386134189
gopubmedrs386134189
geneviewrs386134189
scholarrs386134189
googlers386134189
pharmgkbrs386134189
gwascentralrs386134189
openSNPrs386134189
23andMers386134189
23andMe allrs386134189
SNP Nexus

SNPshotrs386134189
SNPdbers386134189
MSV3drs386134189
GWAS Ctlgrs386134189
Max Magnitude0
ClinVar
Risk rs386134189(AAT,AGGCTCGCCACC;AAT,AGGCTCGCCACC)
Alt rs386134189(AAT,AGGCTCGCCACC;AAT,AGGCTCGCCACC)
Reference rs386134189(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.131705929_131705930insGGCTCGCCACC
CLNSRC ARUP SLC22A5
CLNACC RCV000022314.2,