rs886039467

Orientation

minus

Stabilized

minus

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

Make rs886039467(-;-)

Make rs886039467(-;T)

Reference

GRCh38.p7 38.3/149

Chromosome

17

Position

44859903

Gene

EFTUD2

is a	snp
is	mentioned by
dbSNP	rs886039467
dbSNP (classic)	rs886039467
ClinGen	rs886039467
ebi	rs886039467
HLI	rs886039467
Exac	rs886039467
Gnomad	rs886039467
Varsome	rs886039467
LitVar	rs886039467
Map	rs886039467
PheGenI	rs886039467
Biobank	rs886039467
1000 genomes	rs886039467
hgdp	rs886039467
ensembl	rs886039467
geneview	rs886039467
scholar	rs886039467
google	rs886039467
pharmgkb	rs886039467
gwascentral	rs886039467
openSNP	rs886039467
23andMe	rs886039467
SNPshot	rs886039467
SNPdbe	rs886039467
MSV3d	rs886039467
GWAS Ctlg	rs886039467

Max Magnitude

0

ClinVar
Risk	rs886039467(-;-)
Alt	rs886039467(-;-)
Reference	Rs886039467(T;T)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	EFTUD2
CLNDBN	not provided
Reversed	1
HGVS	NC_000017.10:g.42937271delA
CLNSRC
CLNACC	RCV000254749.1,