rs397508011

Orientation

plus

Stabilized

plus

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

Make rs397508011(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32379382

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397508011
dbSNP (classic)	rs397508011
ClinGen	rs397508011
ebi	rs397508011
HLI	rs397508011
Exac	rs397508011
Gnomad	rs397508011
Varsome	rs397508011
LitVar	rs397508011
Map	rs397508011
PheGenI	rs397508011
Biobank	rs397508011
1000 genomes	rs397508011
hgdp	rs397508011
ensembl	rs397508011
geneview	rs397508011
scholar	rs397508011
google	rs397508011
pharmgkb	rs397508011
gwascentral	rs397508011
openSNP	rs397508011
23andMe	rs397508011
SNPshot	rs397508011
SNPdbe	rs397508011
MSV3d	rs397508011
GWAS Ctlg	rs397508011

Max Magnitude

6

aka c.8820_8823delACAA

ClinVar
Risk	rs397508011(-;-)
Alt	rs397508011(-;-)
Reference	Rs397508011(AAAC;AAAC)
Significance	Untested
Disease	Familial cancer of breast
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast
Reversed	0
HGVS	NC_000013.10:g.32953519_32953522delACAA
CLNSRC	ClinVar
CLNACC	RCV000045634.2,