rs1060502449

Orientation

plus

Stabilized

plus

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

Make rs1060502449(G;T)

Make rs1060502449(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

13

Position

32337461

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs1060502449
dbSNP (classic)	rs1060502449
ClinGen	rs1060502449
ebi	rs1060502449
HLI	rs1060502449
Exac	rs1060502449
Gnomad	rs1060502449
Varsome	rs1060502449
LitVar	rs1060502449
Map	rs1060502449
PheGenI	rs1060502449
Biobank	rs1060502449
1000 genomes	rs1060502449
hgdp	rs1060502449
ensembl	rs1060502449
geneview	rs1060502449
scholar	rs1060502449
google	rs1060502449
pharmgkb	rs1060502449
gwascentral	rs1060502449
openSNP	rs1060502449
23andMe	rs1060502449
SNPshot	rs1060502449
SNPdbe	rs1060502449
MSV3d	rs1060502449
GWAS Ctlg	rs1060502449

Max Magnitude

0

ClinVar
Risk	rs1060502449(T;T)
Alt	rs1060502449(T;T)
Reference	Rs1060502449(G;G)
Significance	Pathogenic
Disease	Hereditary breast and ovarian cancer syndrome
Variation	info
Gene	BRCA2
CLNDBN	Hereditary breast and ovarian cancer syndrome
Reversed	0
HGVS	NC_000013.10:g.32911598G>T
CLNSRC
CLNACC	RCV000456163.1,