rs273897657

Orientation

minus

Stabilized

minus

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

Make rs273897657(-;-)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43115724

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs273897657
dbSNP (classic)	rs273897657
ClinGen	rs273897657
ebi	rs273897657
HLI	rs273897657
Exac	rs273897657
Gnomad	rs273897657
Varsome	rs273897657
LitVar	rs273897657
Map	rs273897657
PheGenI	rs273897657
Biobank	rs273897657
1000 genomes	rs273897657
hgdp	rs273897657
ensembl	rs273897657
geneview	rs273897657
scholar	rs273897657
google	rs273897657
pharmgkb	rs273897657
gwascentral	rs273897657
openSNP	rs273897657
23andMe	rs273897657
SNPshot	rs273897657
SNPdbe	rs273897657
MSV3d	rs273897657
GWAS Ctlg	rs273897657

Max Magnitude

6

aka c.134+2del

ClinVar
Risk	rs273897657(-;-)
Alt	rs273897657(-;-)
Reference	Rs273897657(T;T)
Significance	Other
Disease	Familial cancer of breast Breast-ovarian cancer
Variation	info
Gene	BRCA1
CLNDBN	Familial cancer of breast Breast-ovarian cancer, familial 1
Reversed	1
HGVS	NC_000017.10:g.41267741delA
CLNSRC	Breast Cancer Information Core (BRCA1)
CLNACC	RCV000047429.2, RCV000111850.1,