rs80359165

Orientation

plus

Stabilized

plus

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

Make rs80359165(A;C)

Make rs80359165(C;C)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32379900

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs80359165
dbSNP (classic)	rs80359165
ClinGen	rs80359165
ebi	rs80359165
HLI	rs80359165
Exac	rs80359165
Gnomad	rs80359165
Varsome	rs80359165
LitVar	rs80359165
Map	rs80359165
PheGenI	rs80359165
Biobank	rs80359165
1000 genomes	rs80359165
hgdp	rs80359165
ensembl	rs80359165
geneview	rs80359165
scholar	rs80359165
google	rs80359165
pharmgkb	rs80359165
gwascentral	rs80359165
openSNP	rs80359165
23andMe	rs80359165
SNPshot	rs80359165
SNPdbe	rs80359165
MSV3d	rs80359165
GWAS Ctlg	rs80359165

Max Magnitude

0

ClinVar
Risk	rs80359165(C;C) rs80359165(G;G) rs80359165(T;T)
Alt	rs80359165(C;C) rs80359165(G;G) rs80359165(T;T)
Reference	Rs80359165(A;A)
Significance	Other
Disease	Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome not specified Hereditary cancer-predisposing syndrome
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2 Hereditary breast and ovarian cancer syndrome not specified Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000013.10:g.32954037A>C; NC_000013.10:g.32954037A>G; NC_000013.10:g.32954037A>T
CLNSRC	Ambry Genetics ClinVar
CLNACC	RCV000031794.5, RCV000045717.7, RCV000120368.3, RCV000130861.3, RCV000045718.6, RCV000114048.1, RCV000203635.2, RCV000222955.1, RCV000222210.1,