rs121908888

Orientation

plus

Stabilized

plus

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

Make rs121908888(A;G)

Make rs121908888(G;G)

Reference

GRCh38 38.1/141

Chromosome

5

Position

132384281

Gene

SLC22A5

is a	snp
is	mentioned by
dbSNP	rs121908888
dbSNP (classic)	rs121908888
ClinGen	rs121908888
ebi	rs121908888
HLI	rs121908888
Exac	rs121908888
Gnomad	rs121908888
Varsome	rs121908888
LitVar	rs121908888
Map	rs121908888
PheGenI	rs121908888
Biobank	rs121908888
1000 genomes	rs121908888
hgdp	rs121908888
ensembl	rs121908888
geneview	rs121908888
scholar	rs121908888
google	rs121908888
pharmgkb	rs121908888
gwascentral	rs121908888
openSNP	rs121908888
23andMe	rs121908888
SNPshot	rs121908888
SNPdbe	rs121908888
MSV3d	rs121908888
GWAS Ctlg	rs121908888

Merged from

Rs28939705

Max Magnitude

0

OMIM	603377
Desc
Variant	0012
Related	also

ClinVar
Risk	rs121908888(G;G)
Alt	rs121908888(G;G)
Reference	Rs121908888(A;A)
Significance	Other
Disease	Renal carnitine transport defect not provided
Variation	info
Gene	SLC22A5
CLNDBN	Renal carnitine transport defect not provided
Reversed	0
HGVS	NC_000005.9:g.131719973A>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000006789.5, RCV000186136.3,