rs765835040

Orientation

plus

Stabilized

plus

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

Make rs765835040(C;T)

Make rs765835040(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

44857158

Gene

EFTUD2

is a	snp
is	mentioned by
dbSNP	rs765835040
dbSNP (classic)	rs765835040
ClinGen	rs765835040
ebi	rs765835040
HLI	rs765835040
Exac	rs765835040
Gnomad	rs765835040
Varsome	rs765835040
LitVar	rs765835040
Map	rs765835040
PheGenI	rs765835040
Biobank	rs765835040
1000 genomes	rs765835040
hgdp	rs765835040
ensembl	rs765835040
geneview	rs765835040
scholar	rs765835040
google	rs765835040
pharmgkb	rs765835040
gwascentral	rs765835040
openSNP	rs765835040
23andMe	rs765835040
SNPshot	rs765835040
SNPdbe	rs765835040
MSV3d	rs765835040
GWAS Ctlg	rs765835040

Max Magnitude

0

ClinVar
Risk	rs765835040(A;A) rs765835040(T;T)
Alt	rs765835040(A;A) rs765835040(T;T)
Reference	Rs765835040(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	EFTUD2
CLNDBN	not provided
Reversed	0
HGVS	NC_000017.10:g.42934526C>A
CLNSRC
CLNACC	RCV000479806.1,