rs386134198

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	common in clinvar

Make rs386134198(A;G)

Make rs386134198(G;G)

Reference

GRCh38 38.1/141

Chromosome

5

Position

132384278

Gene

SLC22A5

is a	snp
is	mentioned by
dbSNP	rs386134198
dbSNP (classic)	rs386134198
ClinGen	rs386134198
ebi	rs386134198
HLI	rs386134198
Exac	rs386134198
Gnomad	rs386134198
Varsome	rs386134198
LitVar	rs386134198
Map	rs386134198
PheGenI	rs386134198
Biobank	rs386134198
1000 genomes	rs386134198
hgdp	rs386134198
ensembl	rs386134198
geneview	rs386134198
scholar	rs386134198
google	rs386134198
pharmgkb	rs386134198
gwascentral	rs386134198
openSNP	rs386134198
23andMe	rs386134198
SNPshot	rs386134198
SNPdbe	rs386134198
MSV3d	rs386134198
GWAS Ctlg	rs386134198

Max Magnitude

0

ClinVar
Risk	rs386134198(G;G)
Alt	rs386134198(G;G)
Reference	Rs386134198(A;A)
Significance	Untested
Disease	Renal carnitine transport defect
Variation	info
Gene	SLC22A5
CLNDBN	Renal carnitine transport defect
Reversed	0
HGVS	NC_000005.9:g.131719970A>G
CLNSRC	ARUP SLC22A5
CLNACC	RCV000022330.2,