rs81002899

Orientation

plus

Stabilized

plus

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

Make rs81002899(G;G)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32326615

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs81002899
dbSNP (classic)	rs81002899
ClinGen	rs81002899
ebi	rs81002899
HLI	rs81002899
Exac	rs81002899
Gnomad	rs81002899
Varsome	rs81002899
LitVar	rs81002899
Map	rs81002899
PheGenI	rs81002899
Biobank	rs81002899
1000 genomes	rs81002899
hgdp	rs81002899
ensembl	rs81002899
geneview	rs81002899
scholar	rs81002899
google	rs81002899
pharmgkb	rs81002899
gwascentral	rs81002899
openSNP	rs81002899
23andMe	rs81002899
SNPshot	rs81002899
SNPdbe	rs81002899
MSV3d	rs81002899
GWAS Ctlg	rs81002899

Max Magnitude

6

ClinVar
Risk	rs81002899(A;A) rs81002899(C;C) rs81002899(G;G)
Alt	rs81002899(A;A) rs81002899(C;C) rs81002899(G;G)
Reference	Rs81002899(T;T)
Significance	Pathogenic
Disease	Breast-ovarian cancer not provided Familial cancer of breast Fanconi anemia Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2 not provided Familial cancer of breast Fanconi anemia, complementation group D1 Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome
Reversed	0
HGVS	NC_000013.10:g.32900752T>A; NC_000013.10:g.32900752T>C; NC_000013.10:g.32900752T>G
CLNSRC	Breast Cancer Information Core (BRCA2) OMIM Allelic Variant
CLNACC	RCV000258303.1, RCV000486311.1, RCV000044896.2, RCV000009943.4, RCV000031615.6, RCV000044897.6, RCV000129071.3, RCV000195357.3,