rs786204607

Orientation

minus

Stabilized

minus

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

Make rs786204607(C;T)

Make rs786204607(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

26215149

Gene

HADHA

is a	snp
is	mentioned by
dbSNP	rs786204607
dbSNP (classic)	rs786204607
ClinGen	rs786204607
ebi	rs786204607
HLI	rs786204607
Exac	rs786204607
Gnomad	rs786204607
Varsome	rs786204607
LitVar	rs786204607
Map	rs786204607
PheGenI	rs786204607
Biobank	rs786204607
1000 genomes	rs786204607
hgdp	rs786204607
ensembl	rs786204607
geneview	rs786204607
scholar	rs786204607
google	rs786204607
pharmgkb	rs786204607
gwascentral	rs786204607
openSNP	rs786204607
23andMe	rs786204607
SNPshot	rs786204607
SNPdbe	rs786204607
MSV3d	rs786204607
GWAS Ctlg	rs786204607

Max Magnitude

0

ClinVar
Risk	rs786204607(T;T)
Alt	rs786204607(T;T)
Reference	Rs786204607(C;C)
Significance	Probable-Pathogenic
Disease	Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency not provided
Variation	info
Gene	HADHA
CLNDBN	Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency not provided
Reversed	1
HGVS	NC_000002.11:g.26438018G>A
CLNSRC
CLNACC	RCV000169366.1, RCV000421144.1,