rs876659327

Orientation

minus

Stabilized

minus

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

Make rs876659327(-;G)

Make rs876659327(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

17

Position

43094390

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs876659327
dbSNP (classic)	rs876659327
ClinGen	rs876659327
ebi	rs876659327
HLI	rs876659327
Exac	rs876659327
Gnomad	rs876659327
Varsome	rs876659327
LitVar	rs876659327
Map	rs876659327
PheGenI	rs876659327
Biobank	rs876659327
1000 genomes	rs876659327
hgdp	rs876659327
ensembl	rs876659327
geneview	rs876659327
scholar	rs876659327
google	rs876659327
pharmgkb	rs876659327
gwascentral	rs876659327
openSNP	rs876659327
23andMe	rs876659327
SNPshot	rs876659327
SNPdbe	rs876659327
MSV3d	rs876659327
GWAS Ctlg	rs876659327

Max Magnitude

0

ClinVar
Risk	rs876659327(G;G)
Alt	rs876659327(G;G)
Reference	Rs876659327(-;-)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome not provided Familial cancer of breast
Variation	info
Gene	BRCA1
CLNDBN	Hereditary cancer-predisposing syndrome not provided Familial cancer of breast
Reversed	1
HGVS	NC_000017.10:g.41246408dupC
CLNSRC
CLNACC	RCV000216621.1, RCV000235683.1, RCV000408852.1,