rs770318608

Merged into

rs80359520

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;AATT)	6	BRCA2 variant considered pathogenic for breast cancer
(AATT;AATT)	0	common in clinvar

Make rs770318608(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

13

Position

32339929

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs770318608
dbSNP (classic)	rs770318608
ClinGen	rs770318608
ebi	rs770318608
HLI	rs770318608
Exac	rs770318608
Gnomad	rs770318608
Varsome	rs770318608
LitVar	rs770318608
Map	rs770318608
PheGenI	rs770318608
Biobank	rs770318608
1000 genomes	rs770318608
hgdp	rs770318608
ensembl	rs770318608
geneview	rs770318608
scholar	rs770318608
google	rs770318608
pharmgkb	rs770318608
gwascentral	rs770318608
openSNP	rs770318608
23andMe	rs770318608
SNPshot	rs770318608
SNPdbe	rs770318608
MSV3d	rs770318608
GWAS Ctlg	rs770318608

Status

Merged into rs80359520

Max Magnitude

6

ClinVar
Risk
Alt
Reference	Rs770318608(AATT;AATT)
Significance	Pathogenic
Disease	Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2 Hereditary breast and ovarian cancer syndrome Hereditary cancer-predisposing syndrome not provided
Reversed	0
HGVS	NC_000013.10:g.32914068_32914071delTTAA
CLNSRC	Breast Cancer Information Core (BRCA2) Inc.
CLNACC	RCV000031556.10, RCV000044684.5, RCV000131118.4, RCV000160296.3,