rs869312760

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(ATCGCTTTTCA;ATCGCTTTTCA)	0	common in clinvar
(TCATCGCTTT;TCATCGCTTT)	0	common in clinvar

Make rs869312760(-;-)

Make rs869312760(-;TCGCTTTTCA)

Make rs869312760(TCGCTTTTCA;TCGCTTTTCA)

Reference

GRCh38.p2 38.2/147

Chromosome

13

Position

32370489

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs869312760
dbSNP (classic)	rs869312760
ClinGen	rs869312760
ebi	rs869312760
HLI	rs869312760
Exac	rs869312760
Gnomad	rs869312760
Varsome	rs869312760
LitVar	rs869312760
Map	rs869312760
PheGenI	rs869312760
Biobank	rs869312760
1000 genomes	rs869312760
hgdp	rs869312760
ensembl	rs869312760
geneview	rs869312760
scholar	rs869312760
google	rs869312760
pharmgkb	rs869312760
gwascentral	rs869312760
openSNP	rs869312760
23andMe	rs869312760
SNPshot	rs869312760
SNPdbe	rs869312760
MSV3d	rs869312760
GWAS Ctlg	rs869312760

Max Magnitude

0

ClinVar
Risk	rs869312760(-;-)
Alt	rs869312760(-;-)
Reference	Rs869312760(TCATCGCTTT;TCATCGCTTT)
Significance	Pathogenic
Disease	Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 1
Reversed	0
HGVS	NC_000013.10:g.32944626_32944635delTCGCTTTTCA
CLNSRC
CLNACC	RCV000210188.1,