rs397507636

Orientation

plus

Stabilized

plus

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

Make rs397507636(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32336992

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507636
dbSNP (classic)	rs397507636
ClinGen	rs397507636
ebi	rs397507636
HLI	rs397507636
Exac	rs397507636
Gnomad	rs397507636
Varsome	rs397507636
LitVar	rs397507636
Map	rs397507636
PheGenI	rs397507636
Biobank	rs397507636
1000 genomes	rs397507636
hgdp	rs397507636
ensembl	rs397507636
geneview	rs397507636
scholar	rs397507636
google	rs397507636
pharmgkb	rs397507636
gwascentral	rs397507636
openSNP	rs397507636
23andMe	rs397507636
SNPshot	rs397507636
SNPdbe	rs397507636
MSV3d	rs397507636
GWAS Ctlg	rs397507636

Max Magnitude

6

aka c.2637_2638delTG (p.Glu880fs)

ClinVar
Risk	rs397507636(-;-)
Alt	rs397507636(-;-)
Reference	Rs397507636(TG;TG)
Significance	Untested
Disease	Familial cancer of breast
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast
Reversed	0
HGVS	NC_000013.10:g.32911129_32911130delTG
CLNSRC	ClinVar
CLNACC	RCV000044030.2,