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rs386134206

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs386134206(C;T)
Make rs386134206(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position132385367
GeneSLC22A5
is asnp
is mentioned by
dbSNPrs386134206
ebirs386134206
HLIrs386134206
Exacrs386134206
Varsomers386134206
Maprs386134206
PheGenIrs386134206
hapmaprs386134206
1000 genomesrs386134206
hgdprs386134206
ensemblrs386134206
gopubmedrs386134206
geneviewrs386134206
scholarrs386134206
googlers386134206
pharmgkbrs386134206
gwascentralrs386134206
openSNPrs386134206
23andMers386134206
23andMe allrs386134206
SNP Nexus

SNPshotrs386134206
SNPdbers386134206
MSV3drs386134206
GWAS Ctlgrs386134206
Max Magnitude0
ClinVar
Risk rs386134206(T;T)
Alt rs386134206(T;T)
Reference rs386134206(C;C)
Significance Untested
Disease Renal carnitine transport defect
Variation info
Gene SLC22A5
CLNDBN Renal carnitine transport defect
Reversed 0
HGVS NC_000005.9:g.131721059C>T
CLNSRC ARUP SLC22A5
CLNACC RCV000022349.2,