rs397507727

Orientation

plus

Stabilized

plus

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

Make rs397507727(T;T)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32338907

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507727
ClinGen	rs397507727
ebi	rs397507727
HLI	rs397507727
Exac	rs397507727
Varsome	rs397507727
Map	rs397507727
PheGenI	rs397507727
hapmap	rs397507727
1000 genomes	rs397507727
hgdp	rs397507727
ensembl	rs397507727
gopubmed	rs397507727
geneview	rs397507727
scholar	rs397507727
google	rs397507727
pharmgkb	rs397507727
gwascentral	rs397507727
openSNP	rs397507727
23andMe	rs397507727
23andMe all	rs397507727
SNP Nexus
SNPshot	rs397507727
SNPdbe	rs397507727
MSV3d	rs397507727
GWAS Ctlg	rs397507727

Max Magnitude

6

ClinVar
Risk	rs397507727(T;T)
Alt	rs397507727(T;T)
Reference	Rs397507727(G;G)
Significance	Pathogenic
Disease	Familial cancer of breast Breast-ovarian cancer not provided
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast Breast-ovarian cancer, familial 2 not provided
Reversed	0
HGVS	NC_000013.10:g.32913044G>T
CLNSRC	ClinVar
CLNACC	RCV000044438.2, RCV000241077.1, RCV000480220.1,