rs387906564

Merged into

rs80357571

Orientation

minus

Stabilized

minus

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

Make rs387906564(-;-)

Make rs387906564(-;T)

Reference

GRCh38 38.1/142

Chromosome

17

Position

43091906

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs387906564
dbSNP (classic)	rs387906564
ClinGen	rs387906564
ebi	rs387906564
HLI	rs387906564
Exac	rs387906564
Gnomad	rs387906564
Varsome	rs387906564
LitVar	rs387906564
Map	rs387906564
PheGenI	rs387906564
Biobank	rs387906564
1000 genomes	rs387906564
hgdp	rs387906564
ensembl	rs387906564
geneview	rs387906564
scholar	rs387906564
google	rs387906564
pharmgkb	rs387906564
gwascentral	rs387906564
openSNP	rs387906564
23andMe	rs387906564
SNPshot	rs387906564
SNPdbe	rs387906564
MSV3d	rs387906564
GWAS Ctlg	rs387906564

Status

Merged into rs80357571

Max Magnitude

0

ClinVar
Risk
Alt
Reference	Rs387906564(T;T)
Significance	Pathogenic
Disease	Familial cancer of breast Breast-ovarian cancer
Variation	info
Gene	BRCA1
CLNDBN	Familial cancer of breast Breast-ovarian cancer, familial 1
Reversed	1
HGVS	NC_000017.10:g.41243922delA
CLNSRC	Breast Cancer Information Core (BRCA1) OMIM Allelic Variant
CLNACC	RCV000048261.2, RCV000112140.5,