rs397507766

Orientation

plus

Stabilized

plus

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

Make rs397507766(-;C)

Make rs397507766(C;C)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32326282

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507766
dbSNP (classic)	rs397507766
ClinGen	rs397507766
ebi	rs397507766
HLI	rs397507766
Exac	rs397507766
Gnomad	rs397507766
Varsome	rs397507766
LitVar	rs397507766
Map	rs397507766
PheGenI	rs397507766
Biobank	rs397507766
1000 genomes	rs397507766
hgdp	rs397507766
ensembl	rs397507766
geneview	rs397507766
scholar	rs397507766
google	rs397507766
pharmgkb	rs397507766
gwascentral	rs397507766
openSNP	rs397507766
23andMe	rs397507766
SNPshot	rs397507766
SNPdbe	rs397507766
MSV3d	rs397507766
GWAS Ctlg	rs397507766

Max Magnitude

0

ClinVar
Risk	rs397507766(C;C)
Alt	rs397507766(C;C)
Reference	Rs397507766(-;-)
Significance	Pathogenic
Disease	Familial cancer of breast Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32900419_32900420insC
CLNSRC	ClinVar
CLNACC	RCV000044584.2, RCV000258475.1,