rs397507808

Orientation

plus

Stabilized

plus

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

Make rs397507808(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32340184

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507808
dbSNP (classic)	rs397507808
ClinGen	rs397507808
ebi	rs397507808
HLI	rs397507808
Exac	rs397507808
Gnomad	rs397507808
Varsome	rs397507808
LitVar	rs397507808
Map	rs397507808
PheGenI	rs397507808
Biobank	rs397507808
1000 genomes	rs397507808
hgdp	rs397507808
ensembl	rs397507808
geneview	rs397507808
scholar	rs397507808
google	rs397507808
pharmgkb	rs397507808
gwascentral	rs397507808
openSNP	rs397507808
23andMe	rs397507808
SNPshot	rs397507808
SNPdbe	rs397507808
MSV3d	rs397507808
GWAS Ctlg	rs397507808

Max Magnitude

6

aka c.5829_5830delTA

ClinVar
Risk	rs397507808(-;-)
Alt	rs397507808(-;-)
Reference	Rs397507808(TA;TA)
Significance	Untested
Disease	Familial cancer of breast
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast
Reversed	0
HGVS	NC_000013.10:g.32914321_32914322delTA
CLNSRC	ClinVar
CLNACC	RCV000044767.2,