rs386134206

Orientation

plus

Stabilized

plus

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

Make rs386134206(C;T)

Make rs386134206(T;T)

Reference

GRCh38 38.1/141

Chromosome

5

Position

132385367

Gene

SLC22A5

is a	snp
is	mentioned by
dbSNP	rs386134206
dbSNP (classic)	rs386134206
ClinGen	rs386134206
ebi	rs386134206
HLI	rs386134206
Exac	rs386134206
Gnomad	rs386134206
Varsome	rs386134206
LitVar	rs386134206
Map	rs386134206
PheGenI	rs386134206
Biobank	rs386134206
1000 genomes	rs386134206
hgdp	rs386134206
ensembl	rs386134206
geneview	rs386134206
scholar	rs386134206
google	rs386134206
pharmgkb	rs386134206
gwascentral	rs386134206
openSNP	rs386134206
23andMe	rs386134206
SNPshot	rs386134206
SNPdbe	rs386134206
MSV3d	rs386134206
GWAS Ctlg	rs386134206

Max Magnitude

0

ClinVar
Risk	rs386134206(T;T)
Alt	rs386134206(T;T)
Reference	Rs386134206(C;C)
Significance	Untested
Disease	Renal carnitine transport defect
Variation	info
Gene	SLC22A5
CLNDBN	Renal carnitine transport defect
Reversed	0
HGVS	NC_000005.9:g.131721059C>T
CLNSRC	ARUP SLC22A5
CLNACC	RCV000022349.2,