rs397507609

Merged into

rs80359310

Orientation

plus

Stabilized

plus

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

Make rs397507609(-;A)

Make rs397507609(A;A)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32333293

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507609
dbSNP (classic)	rs397507609
ClinGen	rs397507609
ebi	rs397507609
HLI	rs397507609
Exac	rs397507609
Gnomad	rs397507609
Varsome	rs397507609
LitVar	rs397507609
Map	rs397507609
PheGenI	rs397507609
Biobank	rs397507609
1000 genomes	rs397507609
hgdp	rs397507609
ensembl	rs397507609
geneview	rs397507609
scholar	rs397507609
google	rs397507609
pharmgkb	rs397507609
gwascentral	rs397507609
openSNP	rs397507609
23andMe	rs397507609
SNPshot	rs397507609
SNPdbe	rs397507609
MSV3d	rs397507609
GWAS Ctlg	rs397507609

Status

Merged into rs80359310

Max Magnitude

0

ClinVar
Risk	rs397507609(A;A)
Alt	rs397507609(A;A)
Reference	Rs397507609(;)
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.32907430dupA
CLNSRC	Breast Cancer Information Core (BRCA2)
CLNACC	RCV000043898.2, RCV000112980.3,