rs1719247

Orientation

plus

Stabilized

plus

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

Make rs1719247(C;T)

Make rs1719247(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

15

Position

45328787

is a	snp
is	mentioned by
dbSNP	rs1719247
dbSNP (classic)	rs1719247
ClinGen	rs1719247
ebi	rs1719247
HLI	rs1719247
Exac	rs1719247
Gnomad	rs1719247
Varsome	rs1719247
LitVar	rs1719247
Map	rs1719247
PheGenI	rs1719247
Biobank	rs1719247
1000 genomes	rs1719247
hgdp	rs1719247
ensembl	rs1719247
geneview	rs1719247
scholar	rs1719247
google	rs1719247
pharmgkb	rs1719247
gwascentral	rs1719247
openSNP	rs1719247
23andMe	rs1719247
SNPshot	rs1719247
SNPdbe	rs1719247
MSV3d	rs1719247
GWAS Ctlg	rs1719247

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

ClinVar
Risk	rs1719247(T;T)
Alt	rs1719247(T;T)
Reference	Rs1719247(C;C)
Significance	Drug-response
Disease	hmg coa reductase inhibitors response - Toxicity/ADR simvastatin response - Toxicity/ADR
Variation	info
Gene
CLNDBN	hmg coa reductase inhibitors response - Toxicity/ADR simvastatin response - Toxicity/ADR
Reversed	0
HGVS	NC_000015.9:g.45620985C>T
CLNSRC	PharmGKB Clinical Annotation
CLNACC	RCV000211134.1, RCV000211259.1,