rs397507607

Orientation

plus

Stabilized

plus

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

Make rs397507607(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32333275

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507607
dbSNP (classic)	rs397507607
ClinGen	rs397507607
ebi	rs397507607
HLI	rs397507607
Exac	rs397507607
Gnomad	rs397507607
Varsome	rs397507607
LitVar	rs397507607
Map	rs397507607
PheGenI	rs397507607
Biobank	rs397507607
1000 genomes	rs397507607
hgdp	rs397507607
ensembl	rs397507607
geneview	rs397507607
scholar	rs397507607
google	rs397507607
pharmgkb	rs397507607
gwascentral	rs397507607
openSNP	rs397507607
23andMe	rs397507607
SNPshot	rs397507607
SNPdbe	rs397507607
MSV3d	rs397507607
GWAS Ctlg	rs397507607

Max Magnitude

6

ClinVar
Risk	rs397507607(-;-)
Alt	rs397507607(-;-)
Reference	Rs397507607(TTATA;TTATA)
Significance	Pathogenic
Disease	Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32907412_32907416delTTATA
CLNSRC	ClinVar
CLNACC	RCV000043888.3, RCV000256566.2,