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

rs878853248

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs878853248(-;-)
Make rs878853248(-;C)
Make rs878853248(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position132392530
GeneSLC22A5
is asnp
is mentioned by
dbSNPrs878853248
ebirs878853248
HLIrs878853248
Exacrs878853248
Varsomers878853248
Maprs878853248
PheGenIrs878853248
hapmaprs878853248
1000 genomesrs878853248
hgdprs878853248
ensemblrs878853248
gopubmedrs878853248
geneviewrs878853248
scholarrs878853248
googlers878853248
pharmgkbrs878853248
gwascentralrs878853248
openSNPrs878853248
23andMers878853248
23andMe allrs878853248
SNP Nexus

SNPshotrs878853248
SNPdbers878853248
MSV3drs878853248
GWAS Ctlgrs878853248
Max Magnitude0
ClinVar
Risk rs878853248(C;C)
Alt rs878853248(C;C)
Reference rs878853248(;)
Significance Pathogenic
Disease Renal carnitine transport defect
Variation info
Gene SLC22A5
CLNDBN Renal carnitine transport defect
Reversed 0
HGVS NC_000005.9:g.131728222dupC
CLNSRC
CLNACC RCV000225013.1,