rs771203198

Orientation

plus

Stabilized

plus

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

Make rs771203198(C;C)

Make rs771203198(C;G)

Reference

GRCh38.p7 38.3/149

Chromosome

13

Position

32394750

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs771203198
dbSNP (classic)	rs771203198
ClinGen	rs771203198
ebi	rs771203198
HLI	rs771203198
Exac	rs771203198
Gnomad	rs771203198
Varsome	rs771203198
LitVar	rs771203198
Map	rs771203198
PheGenI	rs771203198
Biobank	rs771203198
1000 genomes	rs771203198
hgdp	rs771203198
ensembl	rs771203198
geneview	rs771203198
scholar	rs771203198
google	rs771203198
pharmgkb	rs771203198
gwascentral	rs771203198
openSNP	rs771203198
23andMe	rs771203198
SNPshot	rs771203198
SNPdbe	rs771203198
MSV3d	rs771203198
GWAS Ctlg	rs771203198

Max Magnitude

6

ClinVar
Risk	rs771203198(A;A) rs771203198(C;C)
Alt	rs771203198(A;A) rs771203198(C;C)
Reference	Rs771203198(G;G)
Significance	Pathogenic
Disease	Neoplasm of breast Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Neoplasm of breast Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32968887G>A
CLNSRC
CLNACC	RCV000240700.1, RCV000256794.2,