rs886038117

Merged into

rs80359479

Orientation

plus

Stabilized

plus

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

Make rs886038117(-;-)

Reference

GRCh38.p7 38.3/149

Chromosome

13

Position

32339425

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs886038117
dbSNP (classic)	rs886038117
ClinGen	rs886038117
ebi	rs886038117
HLI	rs886038117
Exac	rs886038117
Gnomad	rs886038117
Varsome	rs886038117
LitVar	rs886038117
Map	rs886038117
PheGenI	rs886038117
Biobank	rs886038117
1000 genomes	rs886038117
hgdp	rs886038117
ensembl	rs886038117
geneview	rs886038117
scholar	rs886038117
google	rs886038117
pharmgkb	rs886038117
gwascentral	rs886038117
openSNP	rs886038117
23andMe	rs886038117
SNPshot	rs886038117
SNPdbe	rs886038117
MSV3d	rs886038117
GWAS Ctlg	rs886038117

Status

Merged into rs80359479

Max Magnitude

6

ClinVar
Risk
Alt
Reference	Rs886038117(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.32913562_32913565delAAAA
CLNSRC	Breast Cancer Information Core (BRCA2)
CLNACC	RCV000241229.2,