rs397507596

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(AA;AA)	0	common in clinvar

Make rs397507596(-;-)

Make rs397507596(-;AA)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32333074

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507596
dbSNP (classic)	rs397507596
ClinGen	rs397507596
ebi	rs397507596
HLI	rs397507596
Exac	rs397507596
Gnomad	rs397507596
Varsome	rs397507596
LitVar	rs397507596
Map	rs397507596
PheGenI	rs397507596
Biobank	rs397507596
1000 genomes	rs397507596
hgdp	rs397507596
ensembl	rs397507596
geneview	rs397507596
scholar	rs397507596
google	rs397507596
pharmgkb	rs397507596
gwascentral	rs397507596
openSNP	rs397507596
23andMe	rs397507596
SNPshot	rs397507596
SNPdbe	rs397507596
MSV3d	rs397507596
GWAS Ctlg	rs397507596

Max Magnitude

0

ClinVar
Risk	rs397507596(-;-)
Alt	rs397507596(-;-)
Reference	Rs397507596(AA;AA)
Significance	Untested
Disease	Familial cancer of breast
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast
Reversed	0
HGVS	NC_000013.10:g.32907211_32907212delAA
CLNSRC	ClinVar
CLNACC	RCV000043837.2,