rs796051983

Orientation

plus

Stabilized

plus

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

Make rs796051983(C;T)

Make rs796051983(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

15

Position

40415412

Gene

IVD

is a	snp
is	mentioned by
dbSNP	rs796051983
dbSNP (classic)	rs796051983
ClinGen	rs796051983
ebi	rs796051983
HLI	rs796051983
Exac	rs796051983
Gnomad	rs796051983
Varsome	rs796051983
LitVar	rs796051983
Map	rs796051983
PheGenI	rs796051983
Biobank	rs796051983
1000 genomes	rs796051983
hgdp	rs796051983
ensembl	rs796051983
geneview	rs796051983
scholar	rs796051983
google	rs796051983
pharmgkb	rs796051983
gwascentral	rs796051983
openSNP	rs796051983
23andMe	rs796051983
SNPshot	rs796051983
SNPdbe	rs796051983
MSV3d	rs796051983
GWAS Ctlg	rs796051983

Max Magnitude

0

ClinVar
Risk	rs796051983(T;T)
Alt	rs796051983(T;T)
Reference	Rs796051983(C;C)
Significance	Probable-Pathogenic
Disease	Isovaleryl-CoA dehydrogenase deficiency
Variation	info
Gene	IVD
CLNDBN	Isovaleryl-CoA dehydrogenase deficiency
Reversed	0
HGVS	NC_000015.9:g.40707611C>T
CLNSRC
CLNACC	RCV000412245.1,