rs142761835

Orientation

plus

Stabilized

plus

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

Make rs142761835(A;A)

Make rs142761835(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

15

Position

40410699

Gene

IVD

is a	snp
is	mentioned by
dbSNP	rs142761835
dbSNP (classic)	rs142761835
ClinGen	rs142761835
ebi	rs142761835
HLI	rs142761835
Exac	rs142761835
Gnomad	rs142761835
Varsome	rs142761835
LitVar	rs142761835
Map	rs142761835
PheGenI	rs142761835
Biobank	rs142761835
1000 genomes	rs142761835
hgdp	rs142761835
ensembl	rs142761835
geneview	rs142761835
scholar	rs142761835
google	rs142761835
pharmgkb	rs142761835
gwascentral	rs142761835
openSNP	rs142761835
23andMe	rs142761835
SNPshot	rs142761835
SNPdbe	rs142761835
MSV3d	rs142761835
GWAS Ctlg	rs142761835

Max Magnitude

0

ClinVar
Risk	rs142761835(A;A)
Alt	rs142761835(A;A)
Reference	Rs142761835(G;G)
Significance	Other
Disease	not provided Isovaleryl-CoA dehydrogenase deficiency
Variation	info
Gene	IVD
CLNDBN	not provided Isovaleryl-CoA dehydrogenase deficiency
Reversed	0
HGVS	NC_000015.9:g.40702898G>A
CLNSRC	HGMD
CLNACC	RCV000153385.3, RCV000169054.3,