rs2074511

Orientation

minus

Stabilized

minus

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

Make rs2074511(A;G)

Make rs2074511(G;G)

Reference

GRCh38 38.1/141

Chromosome

6

Position

30921612

Gene

VARS2

is a	snp
is	mentioned by
dbSNP	rs2074511
dbSNP (classic)	rs2074511
ClinGen	rs2074511
ebi	rs2074511
HLI	rs2074511
Exac	rs2074511
Gnomad	rs2074511
Varsome	rs2074511
LitVar	rs2074511
Map	rs2074511
PheGenI	rs2074511
Biobank	rs2074511
1000 genomes	rs2074511
hgdp	rs2074511
ensembl	rs2074511
geneview	rs2074511
scholar	rs2074511
google	rs2074511
pharmgkb	rs2074511
gwascentral	rs2074511
openSNP	rs2074511
23andMe	rs2074511
SNPshot	rs2074511
SNPdbe	rs2074511
MSV3d	rs2074511
GWAS Ctlg	rs2074511

GMAF

0.2994

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

[PMID 20503108] VARS2 V552V variant as prognostic marker in patients with early breast cancer

ClinVar
Risk	rs2074511(G;G)
Alt	rs2074511(G;G)
Reference	Rs2074511(A;A)
Significance	Non-pathogenic
Disease	not specified
Variation	info
Gene	VARS2
CLNDBN	not specified
Reversed	1
HGVS	NC_000006.11:g.30889389T>C
CLNSRC
CLNACC	RCV000443955.1,