rs397507679

Orientation

plus

Stabilized

plus

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

Make rs397507679(TAAAAAG;TAAAAAG)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32338000

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507679
dbSNP (classic)	rs397507679
ClinGen	rs397507679
ebi	rs397507679
HLI	rs397507679
Exac	rs397507679
Gnomad	rs397507679
Varsome	rs397507679
LitVar	rs397507679
Map	rs397507679
PheGenI	rs397507679
Biobank	rs397507679
1000 genomes	rs397507679
hgdp	rs397507679
ensembl	rs397507679
geneview	rs397507679
scholar	rs397507679
google	rs397507679
pharmgkb	rs397507679
gwascentral	rs397507679
openSNP	rs397507679
23andMe	rs397507679
SNPshot	rs397507679
SNPdbe	rs397507679
MSV3d	rs397507679
GWAS Ctlg	rs397507679

Max Magnitude

6

ClinVar
Risk	rs397507679(TAAAAAG;TAAAAAG)
Alt	rs397507679(TAAAAAG;TAAAAAG)
Reference	Rs397507679(GT;GT)
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.32912137_32912138delGTinsTAAAAAG
CLNSRC	ClinVar
CLNACC	RCV000044235.2, RCV000256704.2,