rs150544263

Orientation

plus

Stabilized

plus

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

Make rs150544263(A;A)

Make rs150544263(A;T)

Reference

GRCh38 38.1/141

Chromosome

5

Position

132389012

Gene

SLC22A5

is a	snp
is	mentioned by
dbSNP	rs150544263
dbSNP (classic)	rs150544263
ClinGen	rs150544263
ebi	rs150544263
HLI	rs150544263
Exac	rs150544263
Gnomad	rs150544263
Varsome	rs150544263
LitVar	rs150544263
Map	rs150544263
PheGenI	rs150544263
Biobank	rs150544263
1000 genomes	rs150544263
hgdp	rs150544263
ensembl	rs150544263
geneview	rs150544263
scholar	rs150544263
google	rs150544263
pharmgkb	rs150544263
gwascentral	rs150544263
openSNP	rs150544263
23andMe	rs150544263
SNPshot	rs150544263
SNPdbe	rs150544263
MSV3d	rs150544263
GWAS Ctlg	rs150544263

Max Magnitude

0

ClinVar
Risk	rs150544263(A;A) rs150544263(C;C)
Alt	rs150544263(A;A) rs150544263(C;C)
Reference	Rs150544263(T;T)
Significance	Untested
Disease	not specified Renal carnitine transport defect
Variation	info
Gene	SLC22A5
CLNDBN	not specified Renal carnitine transport defect
Reversed	0
HGVS	NC_000005.9:g.131724704T>A; NC_000005.9:g.131724704T>C
CLNSRC	ARUP SLC22A5
CLNACC	RCV000490211.1, RCV000022361.2,