rs397507901

Orientation

plus

Stabilized

plus

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

Make rs397507901(T;T)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32355040

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507901
dbSNP (classic)	rs397507901
ClinGen	rs397507901
ebi	rs397507901
HLI	rs397507901
Exac	rs397507901
Gnomad	rs397507901
Varsome	rs397507901
LitVar	rs397507901
Map	rs397507901
PheGenI	rs397507901
Biobank	rs397507901
1000 genomes	rs397507901
hgdp	rs397507901
ensembl	rs397507901
geneview	rs397507901
scholar	rs397507901
google	rs397507901
pharmgkb	rs397507901
gwascentral	rs397507901
openSNP	rs397507901
23andMe	rs397507901
SNPshot	rs397507901
SNPdbe	rs397507901
MSV3d	rs397507901
GWAS Ctlg	rs397507901

Max Magnitude

6

aka c.7187dupT

ClinVar
Risk	rs397507901(T;T)
Alt	rs397507901(T;T)
Reference	Rs397507901(-;-)
Significance	Untested
Disease	Familial cancer of breast
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast
Reversed	0
HGVS	NC_000013.10:g.32929177dupT
CLNSRC	ClinVar
CLNACC	RCV000045159.2,