rs397507400

Orientation

plus

Stabilized

plus

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

Make rs397507400(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32332304

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507400
dbSNP (classic)	rs397507400
ClinGen	rs397507400
ebi	rs397507400
HLI	rs397507400
Exac	rs397507400
Gnomad	rs397507400
Varsome	rs397507400
LitVar	rs397507400
Map	rs397507400
PheGenI	rs397507400
Biobank	rs397507400
1000 genomes	rs397507400
hgdp	rs397507400
ensembl	rs397507400
geneview	rs397507400
scholar	rs397507400
google	rs397507400
pharmgkb	rs397507400
gwascentral	rs397507400
openSNP	rs397507400
23andMe	rs397507400
SNPshot	rs397507400
SNPdbe	rs397507400
MSV3d	rs397507400
GWAS Ctlg	rs397507400

Max Magnitude

6

ClinVar
Risk	rs397507400(-;-)
Alt	rs397507400(-;-)
Reference	Rs397507400(TAAAG;TAAAG)
Significance	Pathogenic
Disease	Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32906441_32906445delGTAAA
CLNSRC	ClinVar
CLNACC	RCV000031731.4,