rs80358985

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs80358985(C;T)

Make rs80358985(T;T)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32356557

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs80358985
dbSNP (classic)	rs80358985
ClinGen	rs80358985
ebi	rs80358985
HLI	rs80358985
Exac	rs80358985
Gnomad	rs80358985
Varsome	rs80358985
LitVar	rs80358985
Map	rs80358985
PheGenI	rs80358985
Biobank	rs80358985
1000 genomes	rs80358985
hgdp	rs80358985
ensembl	rs80358985
geneview	rs80358985
scholar	rs80358985
google	rs80358985
pharmgkb	rs80358985
gwascentral	rs80358985
openSNP	rs80358985
23andMe	rs80358985
SNPshot	rs80358985
SNPdbe	rs80358985
MSV3d	rs80358985
GWAS Ctlg	rs80358985

Max Magnitude

0

ClinVar
Risk	rs80358985(T;T)
Alt	rs80358985(T;T)
Reference	Rs80358985(C;C)
Significance	Other
Disease	Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome Hereditary cancer-predisposing syndrome not specified
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2 Hereditary breast and ovarian cancer syndrome Hereditary cancer-predisposing syndrome not specified
Reversed	0
HGVS	NC_000013.10:g.32930694C>T
CLNSRC	ClinVar
CLNACC	RCV000031686.6, RCV000045249.5, RCV000162600.2, RCV000212261.2,