rs397507706

Orientation

plus

Stabilized

plus

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

Make rs397507706(A;A)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32338456

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507706
dbSNP (classic)	rs397507706
ClinGen	rs397507706
ebi	rs397507706
HLI	rs397507706
Exac	rs397507706
Gnomad	rs397507706
Varsome	rs397507706
LitVar	rs397507706
Map	rs397507706
PheGenI	rs397507706
Biobank	rs397507706
1000 genomes	rs397507706
hgdp	rs397507706
ensembl	rs397507706
geneview	rs397507706
scholar	rs397507706
google	rs397507706
pharmgkb	rs397507706
gwascentral	rs397507706
openSNP	rs397507706
23andMe	rs397507706
SNPshot	rs397507706
SNPdbe	rs397507706
MSV3d	rs397507706
GWAS Ctlg	rs397507706

Max Magnitude

6

rs397507706 has merged into rs397507705

ClinVar
Risk	rs397507706(A;A)
Alt	rs397507706(A;A)
Reference	Rs397507706(-;-)
Significance	Untested
Disease	Familial cancer of breast
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast
Reversed	0
HGVS	NC_000013.10:g.32912593dupA
CLNSRC	ClinVar
CLNACC	RCV000044351.2,