rs886038193

Merged into

rs80359762

Orientation

plus

Stabilized

plus

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

Make rs886038193(-;-)

Reference

GRCh38.p7 38.3/149

Chromosome

13

Position

32394861

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs886038193
dbSNP (classic)	rs886038193
ClinGen	rs886038193
ebi	rs886038193
HLI	rs886038193
Exac	rs886038193
Gnomad	rs886038193
Varsome	rs886038193
LitVar	rs886038193
Map	rs886038193
PheGenI	rs886038193
Biobank	rs886038193
1000 genomes	rs886038193
hgdp	rs886038193
ensembl	rs886038193
geneview	rs886038193
scholar	rs886038193
google	rs886038193
pharmgkb	rs886038193
gwascentral	rs886038193
openSNP	rs886038193
23andMe	rs886038193
SNPshot	rs886038193
SNPdbe	rs886038193
MSV3d	rs886038193
GWAS Ctlg	rs886038193

Status

Merged into rs80359762

Max Magnitude

6

rs886038193 has merged into rs80359762

ClinVar
Risk
Alt
Reference	Rs886038193(TT;TT)
Significance	Pathogenic
Disease	Familial cancer of breast Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32968998_32968999delTT
CLNSRC	Breast Cancer Information Core (BRCA2)
CLNACC	RCV000045817.2, RCV000241070.2,