rs1057520673

Orientation

minus

Stabilized

minus

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

Make rs1057520673(C;T)

Make rs1057520673(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

44860033

Gene

EFTUD2

is a	snp
is	mentioned by
dbSNP	rs1057520673
dbSNP (classic)	rs1057520673
ClinGen	rs1057520673
ebi	rs1057520673
HLI	rs1057520673
Exac	rs1057520673
Gnomad	rs1057520673
Varsome	rs1057520673
LitVar	rs1057520673
Map	rs1057520673
PheGenI	rs1057520673
Biobank	rs1057520673
1000 genomes	rs1057520673
hgdp	rs1057520673
ensembl	rs1057520673
geneview	rs1057520673
scholar	rs1057520673
google	rs1057520673
pharmgkb	rs1057520673
gwascentral	rs1057520673
openSNP	rs1057520673
23andMe	rs1057520673
SNPshot	rs1057520673
SNPdbe	rs1057520673
MSV3d	rs1057520673
GWAS Ctlg	rs1057520673

Max Magnitude

0

ClinVar
Risk	rs1057520673(T;T)
Alt	rs1057520673(T;T)
Reference	Rs1057520673(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	EFTUD2
CLNDBN	not provided
Reversed	1
HGVS	NC_000017.10:g.42937401G>A
CLNSRC
CLNACC	RCV000431548.1,