rs397507895

Orientation

plus

Stabilized

plus

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

Make rs397507895(ATTTGTATGAACATCTGAC;ATTTGTATGAACATCTGAC)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32354953

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507895
dbSNP (classic)	rs397507895
ClinGen	rs397507895
ebi	rs397507895
HLI	rs397507895
Exac	rs397507895
Gnomad	rs397507895
Varsome	rs397507895
LitVar	rs397507895
Map	rs397507895
PheGenI	rs397507895
Biobank	rs397507895
1000 genomes	rs397507895
hgdp	rs397507895
ensembl	rs397507895
geneview	rs397507895
scholar	rs397507895
google	rs397507895
pharmgkb	rs397507895
gwascentral	rs397507895
openSNP	rs397507895
23andMe	rs397507895
SNPshot	rs397507895
SNPdbe	rs397507895
MSV3d	rs397507895
GWAS Ctlg	rs397507895

Max Magnitude

6

aka c.7082_7100dupATTTGTATGAACATCTGAC

ClinVar
Risk	rs397507895(CATTTGTATGAACATCTGA;CATTTGTATGAACATCTGA)
Alt	rs397507895(CATTTGTATGAACATCTGA;CATTTGTATGAACATCTGA)
Reference	Rs397507895(-;-)
Significance	Untested
Disease	Familial cancer of breast
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast
Reversed	0
HGVS	NC_000013.10:g.32929072_32929090dup19
CLNSRC	ClinVar
CLNACC	RCV000045138.2,