rs776428695

Orientation

plus

Stabilized

plus

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

Make rs776428695(C;T)

Make rs776428695(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

4

Position

158699093

Gene

ETFDH

is a	snp
is	mentioned by
dbSNP	rs776428695
dbSNP (classic)	rs776428695
ClinGen	rs776428695
ebi	rs776428695
HLI	rs776428695
Exac	rs776428695
Gnomad	rs776428695
Varsome	rs776428695
LitVar	rs776428695
Map	rs776428695
PheGenI	rs776428695
Biobank	rs776428695
1000 genomes	rs776428695
hgdp	rs776428695
ensembl	rs776428695
geneview	rs776428695
scholar	rs776428695
google	rs776428695
pharmgkb	rs776428695
gwascentral	rs776428695
openSNP	rs776428695
23andMe	rs776428695
SNPshot	rs776428695
SNPdbe	rs776428695
MSV3d	rs776428695
GWAS Ctlg	rs776428695

Max Magnitude

0

ClinVar
Risk	rs776428695(T;T)
Alt	rs776428695(T;T)
Reference	Rs776428695(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	ETFDH
CLNDBN	not provided
Reversed	0
HGVS	NC_000004.11:g.159620245C>T
CLNSRC
CLNACC	RCV000185898.2,