rs398122710

Orientation

plus

Stabilized

plus

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

Make rs398122710(A;A)

Make rs398122710(A;G)

Reference

GRCh38.p7 38.3/149

Chromosome

13

Position

32371100

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs398122710
dbSNP (classic)	rs398122710
ClinGen	rs398122710
ebi	rs398122710
HLI	rs398122710
Exac	rs398122710
Gnomad	rs398122710
Varsome	rs398122710
LitVar	rs398122710
Map	rs398122710
PheGenI	rs398122710
Biobank	rs398122710
1000 genomes	rs398122710
hgdp	rs398122710
ensembl	rs398122710
geneview	rs398122710
scholar	rs398122710
google	rs398122710
pharmgkb	rs398122710
gwascentral	rs398122710
openSNP	rs398122710
23andMe	rs398122710
SNPshot	rs398122710
SNPdbe	rs398122710
MSV3d	rs398122710
GWAS Ctlg	rs398122710

Max Magnitude

0

ClinVar
Risk	rs398122710(A;A)
Alt	rs398122710(A;A)
Reference	Rs398122710(G;G)
Significance	Probable-Pathogenic
Disease	Breast-ovarian cancer Hereditary cancer-predisposing syndrome Neoplasm of breast
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome Neoplasm of breast
Reversed	0
HGVS	NC_000013.10:g.32945237G>A
CLNSRC
CLNACC	RCV000077638.2, RCV000131955.2, RCV000240702.1,