rs886037968

Merged into

rs80357803

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(T;T)	0	common in clinvar

Make rs886037968(-;-)

Make rs886037968(-;T)

Reference

GRCh38.p7 38.3/149

Chromosome

17

Position

43124032

Gene	BRCA1, NBR2

is a	snp
is	mentioned by
dbSNP	rs886037968
dbSNP (classic)	rs886037968
ClinGen	rs886037968
ebi	rs886037968
HLI	rs886037968
Exac	rs886037968
Gnomad	rs886037968
Varsome	rs886037968
LitVar	rs886037968
Map	rs886037968
PheGenI	rs886037968
Biobank	rs886037968
1000 genomes	rs886037968
hgdp	rs886037968
ensembl	rs886037968
geneview	rs886037968
scholar	rs886037968
google	rs886037968
pharmgkb	rs886037968
gwascentral	rs886037968
openSNP	rs886037968
23andMe	rs886037968
SNPshot	rs886037968
SNPdbe	rs886037968
MSV3d	rs886037968
GWAS Ctlg	rs886037968

Status

Merged into rs80357803

Max Magnitude

0

ClinVar
Risk
Alt
Reference	Rs886037968(T;T)
Significance	Pathogenic
Disease	Familial cancer of breast Breast-ovarian cancer
Variation	info
Gene	NBR2 BRCA1
CLNDBN	Familial cancer of breast Breast-ovarian cancer, familial 1
Reversed	1
HGVS	NC_000017.10:g.41276049delA
CLNSRC	Breast Cancer Information Core (BRCA1)
CLNACC	RCV000049079.2, RCV000241026.2,