rs786203663

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(TGTGG;TGTGG)	0	common in clinvar

Make rs786203663(AGTGA;AGTGA)

Make rs786203663(AGTGA;TGTGG)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

43049164

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs786203663
dbSNP (classic)	rs786203663
ClinGen	rs786203663
ebi	rs786203663
HLI	rs786203663
Exac	rs786203663
Gnomad	rs786203663
Varsome	rs786203663
LitVar	rs786203663
Map	rs786203663
PheGenI	rs786203663
Biobank	rs786203663
1000 genomes	rs786203663
hgdp	rs786203663
ensembl	rs786203663
geneview	rs786203663
scholar	rs786203663
google	rs786203663
pharmgkb	rs786203663
gwascentral	rs786203663
openSNP	rs786203663
23andMe	rs786203663
SNPshot	rs786203663
SNPdbe	rs786203663
MSV3d	rs786203663
GWAS Ctlg	rs786203663

Max Magnitude

0

ClinVar
Risk	rs786203663(AGTGA;AGTGA)
Alt	rs786203663(AGTGA;AGTGA)
Reference	Rs786203663(TGTGG;TGTGG)
Significance	Pathogenic
Disease	not provided Hereditary cancer-predisposing syndrome Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome
Variation	info
Gene	BRCA1
CLNDBN	not provided Hereditary cancer-predisposing syndrome Breast-ovarian cancer, familial 1 Hereditary breast and ovarian cancer syndrome
Reversed	1
HGVS	NC_000017.10:g.41201181_41201185delCCACAinsTCACT
CLNSRC
CLNACC	RCV000159931.2, RCV000167071.1, RCV000239024.1, RCV000471387.1,