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rs150544263

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs150544263(A;A)
Make rs150544263(A;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position132389012
GeneSLC22A5
is asnp
is mentioned by
dbSNPrs150544263
ebirs150544263
HLIrs150544263
Exacrs150544263
Varsomers150544263
Maprs150544263
PheGenIrs150544263
hapmaprs150544263
1000 genomesrs150544263
hgdprs150544263
ensemblrs150544263
gopubmedrs150544263
geneviewrs150544263
scholarrs150544263
googlers150544263
pharmgkbrs150544263
gwascentralrs150544263
openSNPrs150544263
23andMers150544263
23andMe allrs150544263
SNP Nexus

SNPshotrs150544263
SNPdbers150544263
MSV3drs150544263
GWAS Ctlgrs150544263
Max Magnitude0
ClinVar
Risk rs150544263(A,C;A,C)
Alt rs150544263(A,C;A,C)
Reference rs150544263(T;T)
Significance Untested
Disease Renal carnitine transport defect
Variation info
Gene SLC22A5
CLNDBN Renal carnitine transport defect
Reversed 0
HGVS NC_000005.9:g.131724704T>C
CLNSRC ARUP SLC22A5
CLNACC RCV000022361.2,