rs876659614

Orientation

minus

Stabilized

minus

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

Make rs876659614(C;T)

Make rs876659614(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

17

Position

43099880

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs876659614
dbSNP (classic)	rs876659614
ClinGen	rs876659614
ebi	rs876659614
HLI	rs876659614
Exac	rs876659614
Gnomad	rs876659614
Varsome	rs876659614
LitVar	rs876659614
Map	rs876659614
PheGenI	rs876659614
Biobank	rs876659614
1000 genomes	rs876659614
hgdp	rs876659614
ensembl	rs876659614
geneview	rs876659614
scholar	rs876659614
google	rs876659614
pharmgkb	rs876659614
gwascentral	rs876659614
openSNP	rs876659614
23andMe	rs876659614
SNPshot	rs876659614
SNPdbe	rs876659614
MSV3d	rs876659614
GWAS Ctlg	rs876659614

Max Magnitude

0

ClinVar
Risk	rs876659614(A;A) rs876659614(T;T)
Alt	rs876659614(A;A) rs876659614(T;T)
Reference	Rs876659614(C;C)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome
Variation	info
Gene	BRCA1
CLNDBN	Hereditary cancer-predisposing syndrome Breast-ovarian cancer, familial 1 Hereditary breast and ovarian cancer syndrome
Reversed	1
HGVS	NC_000017.10:g.41251897G>A; NC_000017.10:g.41251897G>T
CLNSRC
CLNACC	RCV000219699.1, RCV000238612.1, RCV000214368.1, RCV000463464.1,