rs749855263

Orientation

plus

Stabilized

plus

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

Make rs749855263(A;A)

Make rs749855263(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

44862778

Gene

EFTUD2

is a	snp
is	mentioned by
dbSNP	rs749855263
dbSNP (classic)	rs749855263
ClinGen	rs749855263
ebi	rs749855263
HLI	rs749855263
Exac	rs749855263
Gnomad	rs749855263
Varsome	rs749855263
LitVar	rs749855263
Map	rs749855263
PheGenI	rs749855263
Biobank	rs749855263
1000 genomes	rs749855263
hgdp	rs749855263
ensembl	rs749855263
geneview	rs749855263
scholar	rs749855263
google	rs749855263
pharmgkb	rs749855263
gwascentral	rs749855263
openSNP	rs749855263
23andMe	rs749855263
SNPshot	rs749855263
SNPdbe	rs749855263
MSV3d	rs749855263
GWAS Ctlg	rs749855263

Max Magnitude

0

ClinVar
Risk	rs749855263(A;A)
Alt	rs749855263(A;A)
Reference	Rs749855263(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	EFTUD2
CLNDBN	not provided
Reversed	0
HGVS	NC_000017.10:g.42940146G>T
CLNSRC
CLNACC	RCV000494392.1,