rs397507687

Orientation

plus

Stabilized

plus

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

Make rs397507687(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32316497

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507687
dbSNP (classic)	rs397507687
ClinGen	rs397507687
ebi	rs397507687
HLI	rs397507687
Exac	rs397507687
Gnomad	rs397507687
Varsome	rs397507687
LitVar	rs397507687
Map	rs397507687
PheGenI	rs397507687
Biobank	rs397507687
1000 genomes	rs397507687
hgdp	rs397507687
ensembl	rs397507687
geneview	rs397507687
scholar	rs397507687
google	rs397507687
pharmgkb	rs397507687
gwascentral	rs397507687
openSNP	rs397507687
23andMe	rs397507687
SNPshot	rs397507687
SNPdbe	rs397507687
MSV3d	rs397507687
GWAS Ctlg	rs397507687

Max Magnitude

6

ClinVar
Risk	rs397507687(-;-)
Alt	rs397507687(-;-)
Reference	Rs397507687(TTTTGAAA;TTTTGAAA)
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.32890634_32890641delGAAATTTT
CLNSRC	ClinVar
CLNACC	RCV000044269.2, RCV000256827.2,