rs876660194

Orientation

minus

Stabilized

minus

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

Make rs876660194(A;A)

Reference

GRCh38.p2 38.2/147

Chromosome

17

Position

43092241

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs876660194
dbSNP (classic)	rs876660194
ClinGen	rs876660194
ebi	rs876660194
HLI	rs876660194
Exac	rs876660194
Gnomad	rs876660194
Varsome	rs876660194
LitVar	rs876660194
Map	rs876660194
PheGenI	rs876660194
Biobank	rs876660194
1000 genomes	rs876660194
hgdp	rs876660194
ensembl	rs876660194
geneview	rs876660194
scholar	rs876660194
google	rs876660194
pharmgkb	rs876660194
gwascentral	rs876660194
openSNP	rs876660194
23andMe	rs876660194
SNPshot	rs876660194
SNPdbe	rs876660194
MSV3d	rs876660194
GWAS Ctlg	rs876660194

Max Magnitude

6

ClinVar
Risk	rs876660194(A;A)
Alt	rs876660194(A;A)
Reference	Rs876660194(-;-)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Breast-ovarian cancer
Variation	info
Gene	BRCA1
CLNDBN	Hereditary cancer-predisposing syndrome Breast-ovarian cancer, familial 1
Reversed	1
HGVS	NC_000017.10:g.41244259dupT
CLNSRC
CLNACC	RCV000221558.1, RCV000257391.2,