rs886038088

Merged into

rs797044986

Orientation

plus

Stabilized

plus

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

Make rs886038088(A;A)

Reference

GRCh38.p7 38.3/149

Chromosome

13

Position

32337948

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs886038088
dbSNP (classic)	rs886038088
ClinGen	rs886038088
ebi	rs886038088
HLI	rs886038088
Exac	rs886038088
Gnomad	rs886038088
Varsome	rs886038088
LitVar	rs886038088
Map	rs886038088
PheGenI	rs886038088
Biobank	rs886038088
1000 genomes	rs886038088
hgdp	rs886038088
ensembl	rs886038088
geneview	rs886038088
scholar	rs886038088
google	rs886038088
pharmgkb	rs886038088
gwascentral	rs886038088
openSNP	rs886038088
23andMe	rs886038088
SNPshot	rs886038088
SNPdbe	rs886038088
MSV3d	rs886038088
GWAS Ctlg	rs886038088

Status

Merged into rs797044986

Max Magnitude

6

ClinVar
Risk	rs886038088(A;A)
Alt	rs886038088(A;A)
Reference	Rs886038088(;)
Significance	Pathogenic
Disease	Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32912085dupA
CLNSRC
CLNACC	RCV000241184.2,