rs863224465

Merged into

rs80359473

Orientation

plus

Stabilized

plus

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

Make rs863224465(-;-)

Make rs863224465(-;AAAG)

Reference

GRCh38.p2 38.2/146

Chromosome

13

Position

32339288

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs863224465
dbSNP (classic)	rs863224465
ClinGen	rs863224465
ebi	rs863224465
HLI	rs863224465
Exac	rs863224465
Gnomad	rs863224465
Varsome	rs863224465
LitVar	rs863224465
Map	rs863224465
PheGenI	rs863224465
Biobank	rs863224465
1000 genomes	rs863224465
hgdp	rs863224465
ensembl	rs863224465
geneview	rs863224465
scholar	rs863224465
google	rs863224465
pharmgkb	rs863224465
gwascentral	rs863224465
openSNP	rs863224465
23andMe	rs863224465
SNPshot	rs863224465
SNPdbe	rs863224465
MSV3d	rs863224465
GWAS Ctlg	rs863224465

Status

Merged into rs80359473

Max Magnitude

0

ClinVar
Risk
Alt
Reference	Rs863224465(AAAG;AAAG)
Significance	Pathogenic
Disease	Breast-ovarian cancer not provided Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2 not provided Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome
Reversed	0
HGVS	NC_000013.10:g.32913428_32913431delGAAA
CLNSRC	Breast Cancer Information Core (BRCA2)
CLNACC	RCV000031516.7, RCV000074531.7, RCV000131071.3, RCV000198074.3,