rs794727014

Orientation

plus

Stabilized

plus

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

Make rs794727014(-;-)

Reference

GRCh38.p2 38.2/146

Chromosome

13

Position

32340078

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs794727014
dbSNP (classic)	rs794727014
ClinGen	rs794727014
ebi	rs794727014
HLI	rs794727014
Exac	rs794727014
Gnomad	rs794727014
Varsome	rs794727014
LitVar	rs794727014
Map	rs794727014
PheGenI	rs794727014
Biobank	rs794727014
1000 genomes	rs794727014
hgdp	rs794727014
ensembl	rs794727014
geneview	rs794727014
scholar	rs794727014
google	rs794727014
pharmgkb	rs794727014
gwascentral	rs794727014
openSNP	rs794727014
23andMe	rs794727014
SNPshot	rs794727014
SNPdbe	rs794727014
MSV3d	rs794727014
GWAS Ctlg	rs794727014

Max Magnitude

6

aka c.5723_5727delTAGAT

ClinVar
Risk	rs794727014(-;-)
Alt	rs794727014(-;-)
Reference	Rs794727014(TAGAT;TAGAT)
Significance	Pathogenic
Disease	Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32914215_32914219delTAGAT
CLNSRC
CLNACC	RCV000173957.2,