rs397508022

Orientation

plus

Stabilized

plus

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

Make rs397508022(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32379512

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397508022
dbSNP (classic)	rs397508022
ClinGen	rs397508022
ebi	rs397508022
HLI	rs397508022
Exac	rs397508022
Gnomad	rs397508022
Varsome	rs397508022
LitVar	rs397508022
Map	rs397508022
PheGenI	rs397508022
Biobank	rs397508022
1000 genomes	rs397508022
hgdp	rs397508022
ensembl	rs397508022
geneview	rs397508022
scholar	rs397508022
google	rs397508022
pharmgkb	rs397508022
gwascentral	rs397508022
openSNP	rs397508022
23andMe	rs397508022
SNPshot	rs397508022
SNPdbe	rs397508022
MSV3d	rs397508022
GWAS Ctlg	rs397508022

Max Magnitude

6

aka c.8950delT

ClinVar
Risk	rs397508022(-;-)
Alt	rs397508022(-;-)
Reference	Rs397508022(T;T)
Significance	Untested
Disease	Familial cancer of breast
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast
Reversed	0
HGVS	NC_000013.10:g.32953649delT
CLNSRC	ClinVar
CLNACC	RCV000045664.2,