rs397508026

Orientation

plus

Stabilized

plus

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

Make rs397508026(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32379774

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397508026
dbSNP (classic)	rs397508026
ClinGen	rs397508026
ebi	rs397508026
HLI	rs397508026
Exac	rs397508026
Gnomad	rs397508026
Varsome	rs397508026
LitVar	rs397508026
Map	rs397508026
PheGenI	rs397508026
Biobank	rs397508026
1000 genomes	rs397508026
hgdp	rs397508026
ensembl	rs397508026
geneview	rs397508026
scholar	rs397508026
google	rs397508026
pharmgkb	rs397508026
gwascentral	rs397508026
openSNP	rs397508026
23andMe	rs397508026
SNPshot	rs397508026
SNPdbe	rs397508026
MSV3d	rs397508026
GWAS Ctlg	rs397508026

Max Magnitude

6

ClinVar
Risk	rs397508026(-;-)
Alt	rs397508026(-;-)
Reference	Rs397508026(ATCATCAGATTTAT;ATCATCAGATTTAT)
Significance	Pathogenic
Disease	Familial cancer of breast Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32953911_32953924delCATCAGATTTATAT
CLNSRC	ClinVar
CLNACC	RCV000045678.2, RCV000257752.2,