rs786202791

Orientation

minus

Stabilized

minus

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

Make rs786202791(-;-)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

43092207

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs786202791
dbSNP (classic)	rs786202791
ClinGen	rs786202791
ebi	rs786202791
HLI	rs786202791
Exac	rs786202791
Gnomad	rs786202791
Varsome	rs786202791
LitVar	rs786202791
Map	rs786202791
PheGenI	rs786202791
Biobank	rs786202791
1000 genomes	rs786202791
hgdp	rs786202791
ensembl	rs786202791
geneview	rs786202791
scholar	rs786202791
google	rs786202791
pharmgkb	rs786202791
gwascentral	rs786202791
openSNP	rs786202791
23andMe	rs786202791
SNPshot	rs786202791
SNPdbe	rs786202791
MSV3d	rs786202791
GWAS Ctlg	rs786202791

Max Magnitude

6

ClinVar
Risk	rs786202791(-;-)
Alt	rs786202791(-;-)
Reference	Rs786202791(TA;TA)
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.41244224_41244225delTA
CLNSRC
CLNACC	RCV000165779.1, RCV000241028.1,