rs886038128

Merged into

rs276174861

Orientation

plus

Stabilized

plus

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

Make rs886038128(CC;CC)

Reference

GRCh38.p7 38.3/149

Chromosome

13

Position

32340011

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs886038128
dbSNP (classic)	rs886038128
ClinGen	rs886038128
ebi	rs886038128
HLI	rs886038128
Exac	rs886038128
Gnomad	rs886038128
Varsome	rs886038128
LitVar	rs886038128
Map	rs886038128
PheGenI	rs886038128
Biobank	rs886038128
1000 genomes	rs886038128
hgdp	rs886038128
ensembl	rs886038128
geneview	rs886038128
scholar	rs886038128
google	rs886038128
pharmgkb	rs886038128
gwascentral	rs886038128
openSNP	rs886038128
23andMe	rs886038128
SNPshot	rs886038128
SNPdbe	rs886038128
MSV3d	rs886038128
GWAS Ctlg	rs886038128

Status

Merged into rs276174861

Max Magnitude

6

ClinVar
Risk	rs886038128(CC;CC)
Alt	rs886038128(CC;CC)
Reference	Rs886038128(;)
Significance	Pathogenic
Disease	Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32914147_32914148dupCC
CLNSRC	Breast Cancer Information Core (BRCA2)
CLNACC	RCV000241498.2,