rs397507825

Orientation

plus

Stabilized

plus

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

Make rs397507825(-;-)

Make rs397507825(-;ACAT)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32340415

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507825
dbSNP (classic)	rs397507825
ClinGen	rs397507825
ebi	rs397507825
HLI	rs397507825
Exac	rs397507825
Gnomad	rs397507825
Varsome	rs397507825
LitVar	rs397507825
Map	rs397507825
PheGenI	rs397507825
Biobank	rs397507825
1000 genomes	rs397507825
hgdp	rs397507825
ensembl	rs397507825
geneview	rs397507825
scholar	rs397507825
google	rs397507825
pharmgkb	rs397507825
gwascentral	rs397507825
openSNP	rs397507825
23andMe	rs397507825
SNPshot	rs397507825
SNPdbe	rs397507825
MSV3d	rs397507825
GWAS Ctlg	rs397507825

Max Magnitude

0

ClinVar
Risk	rs397507825(-;-)
Alt	rs397507825(-;-)
Reference	Rs397507825(ACAT;ACAT)
Significance	Untested
Disease	Familial cancer of breast
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast
Reversed	0
HGVS	NC_000013.10:g.32914552_32914555delACAT
CLNSRC	ClinVar
CLNACC	RCV000044829.2,