rs730881614

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;ATGATACGGAAAT)	6	BRCA2 variant considered pathogenic for breast cancer
(ATATGATACGGAA;ATATGATACGGAA)	0	common in clinvar
(ATGATACGGAAAT;ATGATACGGAAAT)	0	common/normal

Make rs730881614(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

13

Position

32363181

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs730881614
dbSNP (classic)	rs730881614
ClinGen	rs730881614
ebi	rs730881614
HLI	rs730881614
Exac	rs730881614
Gnomad	rs730881614
Varsome	rs730881614
LitVar	rs730881614
Map	rs730881614
PheGenI	rs730881614
Biobank	rs730881614
1000 genomes	rs730881614
hgdp	rs730881614
ensembl	rs730881614
geneview	rs730881614
scholar	rs730881614
google	rs730881614
pharmgkb	rs730881614
gwascentral	rs730881614
openSNP	rs730881614
23andMe	rs730881614
SNPshot	rs730881614
SNPdbe	rs730881614
MSV3d	rs730881614
GWAS Ctlg	rs730881614

Max Magnitude

6

ClinVar
Risk	rs730881614(-;-)
Alt	rs730881614(-;-)
Reference	Rs730881614(ATATGATACGGAA;ATATGATACGGAA)
Significance	Pathogenic
Disease	Familial cancer of breast Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32937318_32937330delATGATACGGAAAT
CLNSRC
CLNACC	RCV000160306.1, RCV000241464.1,