rs876659457

Orientation

minus

Stabilized

minus

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

Make rs876659457(A;T)

Make rs876659457(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

17

Position

43092851

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs876659457
dbSNP (classic)	rs876659457
ClinGen	rs876659457
ebi	rs876659457
HLI	rs876659457
Exac	rs876659457
Gnomad	rs876659457
Varsome	rs876659457
LitVar	rs876659457
Map	rs876659457
PheGenI	rs876659457
Biobank	rs876659457
1000 genomes	rs876659457
hgdp	rs876659457
ensembl	rs876659457
geneview	rs876659457
scholar	rs876659457
google	rs876659457
pharmgkb	rs876659457
gwascentral	rs876659457
openSNP	rs876659457
23andMe	rs876659457
SNPshot	rs876659457
SNPdbe	rs876659457
MSV3d	rs876659457
GWAS Ctlg	rs876659457

Max Magnitude

0

ClinVar
Risk	rs876659457(T;T)
Alt	rs876659457(T;T)
Reference	Rs876659457(A;A)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	BRCA1
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000017.10:g.41244868T>A
CLNSRC
CLNACC	RCV000221767.1,