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rs377767445

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs377767445(C;T)
Make rs377767445(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position132370109
GeneMIR4750, SLC22A5
is asnp
is mentioned by
dbSNPrs377767445
ebirs377767445
HLIrs377767445
Exacrs377767445
Varsomers377767445
Maprs377767445
PheGenIrs377767445
hapmaprs377767445
1000 genomesrs377767445
hgdprs377767445
ensemblrs377767445
gopubmedrs377767445
geneviewrs377767445
scholarrs377767445
googlers377767445
pharmgkbrs377767445
gwascentralrs377767445
openSNPrs377767445
23andMers377767445
23andMe allrs377767445
SNP Nexus

SNPshotrs377767445
SNPdbers377767445
MSV3drs377767445
GWAS Ctlgrs377767445
Max Magnitude0
ClinVar
Risk rs377767445(T;T)
Alt rs377767445(T;T)
Reference Rs377767445(C;C)
Significance Untested
Disease Renal carnitine transport defect
Variation info
Gene LOC553103 SLC22A5
CLNDBN Renal carnitine transport defect
Reversed 0
HGVS NC_000005.9:g.131705801C>T
CLNSRC ARUP SLC22A5
CLNACC RCV000022304.2,