rs397507633

Orientation

plus

Stabilized

plus

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

Make rs397507633(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32336951

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507633
dbSNP (classic)	rs397507633
ClinGen	rs397507633
ebi	rs397507633
HLI	rs397507633
Exac	rs397507633
Gnomad	rs397507633
Varsome	rs397507633
LitVar	rs397507633
Map	rs397507633
PheGenI	rs397507633
Biobank	rs397507633
1000 genomes	rs397507633
hgdp	rs397507633
ensembl	rs397507633
geneview	rs397507633
scholar	rs397507633
google	rs397507633
pharmgkb	rs397507633
gwascentral	rs397507633
openSNP	rs397507633
23andMe	rs397507633
SNPshot	rs397507633
SNPdbe	rs397507633
MSV3d	rs397507633
GWAS Ctlg	rs397507633

Max Magnitude

6

aka c.2596_2599delGAAA

ClinVar
Risk	rs397507633(-;-)
Alt	rs397507633(-;-)
Reference	Rs397507633(AAGA;AAGA)
Significance	Untested
Disease	Familial cancer of breast
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast
Reversed	0
HGVS	NC_000013.10:g.32911088_32911091delGAAA
CLNSRC	ClinVar
CLNACC	RCV000044022.2,