rs397507655

Orientation

plus

Stabilized

plus

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

Make rs397507655(T;T)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32337451

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507655
dbSNP (classic)	rs397507655
ClinGen	rs397507655
ebi	rs397507655
HLI	rs397507655
Exac	rs397507655
Gnomad	rs397507655
Varsome	rs397507655
LitVar	rs397507655
Map	rs397507655
PheGenI	rs397507655
Biobank	rs397507655
1000 genomes	rs397507655
hgdp	rs397507655
ensembl	rs397507655
geneview	rs397507655
scholar	rs397507655
google	rs397507655
pharmgkb	rs397507655
gwascentral	rs397507655
openSNP	rs397507655
23andMe	rs397507655
SNPshot	rs397507655
SNPdbe	rs397507655
MSV3d	rs397507655
GWAS Ctlg	rs397507655

Max Magnitude

6

aka c.3096_3110delAGATATTGAAGAACAinsT

ClinVar
Risk	rs397507655(T;T)
Alt	rs397507655(T;T)
Reference	Rs397507655(AGATATTGAAGAACA;AGATATTGAAGAACA)
Significance	Pathogenic
Disease	Familial cancer of breast not provided
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast not provided
Reversed	0
HGVS	NC_000013.10:g.32911588_32911602delAGATATTGAAGAACAinsT
CLNSRC	ClinVar
CLNACC	RCV000044118.2, RCV000481789.1,