rs273902778

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(-;A)	6	BRCA1 variant considered pathogenic for breast cancer
(A;A)	0	common in clinvar

Make rs273902778(-;-)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43124036

Gene	BRCA1, NBR2

is a	snp
is	mentioned by
dbSNP	rs273902778
dbSNP (classic)	rs273902778
ClinGen	rs273902778
ebi	rs273902778
HLI	rs273902778
Exac	rs273902778
Gnomad	rs273902778
Varsome	rs273902778
LitVar	rs273902778
Map	rs273902778
PheGenI	rs273902778
Biobank	rs273902778
1000 genomes	rs273902778
hgdp	rs273902778
ensembl	rs273902778
geneview	rs273902778
scholar	rs273902778
google	rs273902778
pharmgkb	rs273902778
gwascentral	rs273902778
openSNP	rs273902778
23andMe	rs273902778
SNPshot	rs273902778
SNPdbe	rs273902778
MSV3d	rs273902778
GWAS Ctlg	rs273902778

Max Magnitude

6

ClinVar
Risk	rs273902778(-;-)
Alt	rs273902778(-;-)
Reference	Rs273902778(A;A)
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.41276053delT
CLNSRC	Breast Cancer Information Core (BRCA1)
CLNACC	RCV000049073.2, RCV000111664.3,