rs1064793785

Orientation

plus

Stabilized

plus

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

Chromosome

13

Position

32338494

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs1064793785
dbSNP (classic)	rs1064793785
ClinGen	rs1064793785
ebi	rs1064793785
HLI	rs1064793785
Exac	rs1064793785
Gnomad	rs1064793785
Varsome	rs1064793785
LitVar	rs1064793785
Map	rs1064793785
PheGenI	rs1064793785
Biobank	rs1064793785
1000 genomes	rs1064793785
hgdp	rs1064793785
ensembl	rs1064793785
geneview	rs1064793785
scholar	rs1064793785
google	rs1064793785
pharmgkb	rs1064793785
gwascentral	rs1064793785
openSNP	rs1064793785
23andMe	rs1064793785
SNPshot	rs1064793785
SNPdbe	rs1064793785
MSV3d	rs1064793785
GWAS Ctlg	rs1064793785

Max Magnitude

0

ClinVar
Risk	rs1064793785(TT;TT)
Alt	rs1064793785(TT;TT)
Reference	Rs1064793785(-;-)
Significance	Pathogenic
Disease	Familial cancer of breast Breast-ovarian cancer Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome not provided
Reversed	0
HGVS	NC_000013.10:g.32912631_32912632dupTT
CLNSRC	Breast Cancer Information Core (BRCA2)
CLNACC	RCV000044359.2, RCV000113279.2, RCV000130775.2, RCV000483206.2,