rs786202157

Orientation

plus

Stabilized

plus

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

Make rs786202157(AAAG;AAAG)

Reference

GRCh38.p2 38.2/146

Chromosome

13

Position

32341018

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs786202157
dbSNP (classic)	rs786202157
ClinGen	rs786202157
ebi	rs786202157
HLI	rs786202157
Exac	rs786202157
Gnomad	rs786202157
Varsome	rs786202157
LitVar	rs786202157
Map	rs786202157
PheGenI	rs786202157
Biobank	rs786202157
1000 genomes	rs786202157
hgdp	rs786202157
ensembl	rs786202157
geneview	rs786202157
scholar	rs786202157
google	rs786202157
pharmgkb	rs786202157
gwascentral	rs786202157
openSNP	rs786202157
23andMe	rs786202157
SNPshot	rs786202157
SNPdbe	rs786202157
MSV3d	rs786202157
GWAS Ctlg	rs786202157

Max Magnitude

6

ClinVar
Risk	rs786202157(AAAG;AAAG)
Alt	rs786202157(AAAG;AAAG)
Reference	Rs786202157(-;-)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Hereditary cancer-predisposing syndrome Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32915155_32915156insAAAG
CLNSRC
CLNACC	RCV000164833.1, RCV000256587.2,