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rs377767450

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs377767450(C;C)
Make rs377767450(C;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position132370259
GeneMIR4750, SLC22A5
is asnp
is mentioned by
dbSNPrs377767450
ebirs377767450
HLIrs377767450
Exacrs377767450
Varsomers377767450
Maprs377767450
PheGenIrs377767450
hapmaprs377767450
1000 genomesrs377767450
hgdprs377767450
ensemblrs377767450
gopubmedrs377767450
geneviewrs377767450
scholarrs377767450
googlers377767450
pharmgkbrs377767450
gwascentralrs377767450
openSNPrs377767450
23andMers377767450
23andMe allrs377767450
SNP Nexus

SNPshotrs377767450
SNPdbers377767450
MSV3drs377767450
GWAS Ctlgrs377767450
Max Magnitude0
ClinVar
Risk rs377767450(C;C)
Alt rs377767450(C;C)
Reference rs377767450(G;G)
Significance Untested
Disease Renal carnitine transport defect not specified
Variation info
Gene LOC553103 SLC22A5
CLNDBN Renal carnitine transport defect not specified
Reversed 0
HGVS NC_000005.9:g.131705951G>C
CLNSRC ARUP SLC22A5
CLNACC RCV000022311.2, RCV000186133.1,