rs886038097

Merged into

rs431825313

Orientation

plus

Stabilized

plus

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

Make rs886038097(-;-)

Reference

GRCh38.p7 38.3/149

Chromosome

13

Position

32338212

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs886038097
dbSNP (classic)	rs886038097
ClinGen	rs886038097
ebi	rs886038097
HLI	rs886038097
Exac	rs886038097
Gnomad	rs886038097
Varsome	rs886038097
LitVar	rs886038097
Map	rs886038097
PheGenI	rs886038097
Biobank	rs886038097
1000 genomes	rs886038097
hgdp	rs886038097
ensembl	rs886038097
geneview	rs886038097
scholar	rs886038097
google	rs886038097
pharmgkb	rs886038097
gwascentral	rs886038097
openSNP	rs886038097
23andMe	rs886038097
SNPshot	rs886038097
SNPdbe	rs886038097
MSV3d	rs886038097
GWAS Ctlg	rs886038097

Status

Merged into rs431825313

Max Magnitude

6

ClinVar
Risk
Alt
Reference	Rs886038097(AAAA;AAAA)
Significance	Pathogenic
Disease	Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32912349_32912352delAAAA
CLNSRC
CLNACC	RCV000241173.2,