rs386134192

Orientation

plus

Stabilized

plus

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

Make rs386134192(A;G)

Make rs386134192(G;G)

Reference

GRCh38 38.1/141

Chromosome

5

Position

132370316

Gene	LOC553103, SLC22A5

is a	snp
is	mentioned by
dbSNP	rs386134192
dbSNP (classic)	rs386134192
ClinGen	rs386134192
ebi	rs386134192
HLI	rs386134192
Exac	rs386134192
Gnomad	rs386134192
Varsome	rs386134192
LitVar	rs386134192
Map	rs386134192
PheGenI	rs386134192
Biobank	rs386134192
1000 genomes	rs386134192
hgdp	rs386134192
ensembl	rs386134192
geneview	rs386134192
scholar	rs386134192
google	rs386134192
pharmgkb	rs386134192
gwascentral	rs386134192
openSNP	rs386134192
23andMe	rs386134192
SNPshot	rs386134192
SNPdbe	rs386134192
MSV3d	rs386134192
GWAS Ctlg	rs386134192

Max Magnitude

0

ClinVar
Risk	rs386134192(G;G)
Alt	rs386134192(G;G)
Reference	Rs386134192(A;A)
Significance	Untested
Disease	Renal carnitine transport defect
Variation	info
Gene	LOC553103 SLC22A5
CLNDBN	Renal carnitine transport defect
Reversed	0
HGVS	NC_000005.9:g.131706008A>G
CLNSRC	ARUP SLC22A5
CLNACC	RCV000022317.2,