rs886039349

Orientation

minus

Stabilized

minus

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

Make rs886039349(-;-)

Make rs886039349(-;GTCT)

Reference

GRCh38.p7 38.3/149

Chromosome

17

Position

44852423

Gene

EFTUD2

is a	snp
is	mentioned by
dbSNP	rs886039349
dbSNP (classic)	rs886039349
ClinGen	rs886039349
ebi	rs886039349
HLI	rs886039349
Exac	rs886039349
Gnomad	rs886039349
Varsome	rs886039349
LitVar	rs886039349
Map	rs886039349
PheGenI	rs886039349
Biobank	rs886039349
1000 genomes	rs886039349
hgdp	rs886039349
ensembl	rs886039349
geneview	rs886039349
scholar	rs886039349
google	rs886039349
pharmgkb	rs886039349
gwascentral	rs886039349
openSNP	rs886039349
23andMe	rs886039349
SNPshot	rs886039349
SNPdbe	rs886039349
MSV3d	rs886039349
GWAS Ctlg	rs886039349

Max Magnitude

0

ClinVar
Risk	rs886039349(-;-)
Alt	rs886039349(-;-)
Reference	Rs886039349(GTCT;GTCT)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	EFTUD2
CLNDBN	not provided
Reversed	1
HGVS	NC_000017.10:g.42929791_42929794delAGAC
CLNSRC
CLNACC	RCV000254790.1,