rs1060499833

Orientation

plus

Stabilized

plus

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

Make rs1060499833(G;G)

Make rs1060499833(G;T)

Reference

GRCh38.p7 38.3/150

Chromosome

13

Position

32339338

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs1060499833
dbSNP (classic)	rs1060499833
ClinGen	rs1060499833
ebi	rs1060499833
HLI	rs1060499833
Exac	rs1060499833
Gnomad	rs1060499833
Varsome	rs1060499833
LitVar	rs1060499833
Map	rs1060499833
PheGenI	rs1060499833
Biobank	rs1060499833
1000 genomes	rs1060499833
hgdp	rs1060499833
ensembl	rs1060499833
geneview	rs1060499833
scholar	rs1060499833
google	rs1060499833
pharmgkb	rs1060499833
gwascentral	rs1060499833
openSNP	rs1060499833
23andMe	rs1060499833
SNPshot	rs1060499833
SNPdbe	rs1060499833
MSV3d	rs1060499833
GWAS Ctlg	rs1060499833

Max Magnitude

0

ClinVar
Risk	rs1060499833(G;G)
Alt	rs1060499833(G;G)
Reference	Rs1060499833(T;T)
Significance	Pathogenic
Disease	Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32913475T>G
CLNSRC
CLNACC	RCV000469488.1,