Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs2631365

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs2631365(A;G)
Make rs2631365(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position132370257
GeneLOC553103, SLC22A5
is asnp
is mentioned by
dbSNPrs2631365
dbSNP (old)rs2631365
ClinGenrs2631365
ebirs2631365
HLIrs2631365
Exacrs2631365
Gnomadrs2631365
Varsomers2631365
Maprs2631365
PheGenIrs2631365
Biobankrs2631365
1000 genomesrs2631365
hgdprs2631365
ensemblrs2631365
gopubmedrs2631365
geneviewrs2631365
scholarrs2631365
googlers2631365
pharmgkbrs2631365
gwascentralrs2631365
openSNPrs2631365
23andMers2631365
23andMe allrs2631365
SNPshotrs2631365
SNPdbers2631365
MSV3drs2631365
GWAS Ctlgrs2631365
Max Magnitude0

[PMID 28420426OA-icon.png] Genotypes of SLC22A4 and SLC22A5 regulatory loci are predictive of the response of chronic myeloid leukemia patients to imatinib treatment.

ClinVar
Risk rs2631365(G;G)
Alt rs2631365(G;G)
Reference Rs2631365(A;A)
Significance Non-pathogenic
Disease Renal carnitine transport defect not specified
Variation info
Gene LOC553103 SLC22A5
CLNDBN Renal carnitine transport defect not specified
Reversed 1
HGVS NC_000005.9:g.131705949T\x3d; NC_000005.9:g.131705949T>C
CLNSRC
CLNACC RCV000022310.2, RCV000080053.5, RCV000406963.1,