rs397507834

Orientation

plus

Stabilized

plus

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

Make rs397507834(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32340561

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507834
dbSNP (classic)	rs397507834
ClinGen	rs397507834
ebi	rs397507834
HLI	rs397507834
Exac	rs397507834
Gnomad	rs397507834
Varsome	rs397507834
LitVar	rs397507834
Map	rs397507834
PheGenI	rs397507834
Biobank	rs397507834
1000 genomes	rs397507834
hgdp	rs397507834
ensembl	rs397507834
geneview	rs397507834
scholar	rs397507834
google	rs397507834
pharmgkb	rs397507834
gwascentral	rs397507834
openSNP	rs397507834
23andMe	rs397507834
SNPshot	rs397507834
SNPdbe	rs397507834
MSV3d	rs397507834
GWAS Ctlg	rs397507834

Max Magnitude

6

aka c.6206delT

ClinVar
Risk	rs397507834(-;-)
Alt	rs397507834(-;-)
Reference	Rs397507834(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.32914698delT
CLNSRC	ClinVar
CLNACC	RCV000044868.2,