rs786202700

Orientation

plus

Stabilized

plus

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

Make rs786202700(-;-)

Reference

GRCh38.p2 38.2/146

Chromosome

13

Position

32340217

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs786202700
dbSNP (classic)	rs786202700
ClinGen	rs786202700
ebi	rs786202700
HLI	rs786202700
Exac	rs786202700
Gnomad	rs786202700
Varsome	rs786202700
LitVar	rs786202700
Map	rs786202700
PheGenI	rs786202700
Biobank	rs786202700
1000 genomes	rs786202700
hgdp	rs786202700
ensembl	rs786202700
geneview	rs786202700
scholar	rs786202700
google	rs786202700
pharmgkb	rs786202700
gwascentral	rs786202700
openSNP	rs786202700
23andMe	rs786202700
SNPshot	rs786202700
SNPdbe	rs786202700
MSV3d	rs786202700
GWAS Ctlg	rs786202700

Max Magnitude

6

aka c.5862_5863delTT

ClinVar
Risk	rs786202700(-;-)
Alt	rs786202700(-;-)
Reference	Rs786202700(TT;TT)
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.32914354_32914355delTT
CLNSRC
CLNACC	RCV000165639.1, RCV000241377.2,