rs767595162

Orientation

plus

Stabilized

plus

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

Make rs767595162(CA;CA)

Reference

GRCh38.p7 38.3/149

Chromosome

17

Position

43093687

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs767595162
dbSNP (classic)	rs767595162
ClinGen	rs767595162
ebi	rs767595162
HLI	rs767595162
Exac	rs767595162
Gnomad	rs767595162
Varsome	rs767595162
LitVar	rs767595162
Map	rs767595162
PheGenI	rs767595162
Biobank	rs767595162
1000 genomes	rs767595162
hgdp	rs767595162
ensembl	rs767595162
geneview	rs767595162
scholar	rs767595162
google	rs767595162
pharmgkb	rs767595162
gwascentral	rs767595162
openSNP	rs767595162
23andMe	rs767595162
SNPshot	rs767595162
SNPdbe	rs767595162
MSV3d	rs767595162
GWAS Ctlg	rs767595162

Max Magnitude

6

ClinVar
Risk	rs767595162(AC;AC)
Alt	rs767595162(AC;AC)
Reference	Rs767595162(-;-)
Significance	Pathogenic
Disease	Breast-ovarian cancer
Variation	info
Gene	BRCA1
CLNDBN	Breast-ovarian cancer, familial 1
Reversed	0
HGVS	NC_000017.10:g.41245705_41245706dupAC
CLNSRC
CLNACC	RCV000241272.1,