rs397509009

Merged into

rs80357942

Orientation

minus

Stabilized

minus

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

Make rs397509009(-;A)

Make rs397509009(A;A)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43092781

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397509009
dbSNP (classic)	rs397509009
ClinGen	rs397509009
ebi	rs397509009
HLI	rs397509009
Exac	rs397509009
Gnomad	rs397509009
Varsome	rs397509009
LitVar	rs397509009
Map	rs397509009
PheGenI	rs397509009
Biobank	rs397509009
1000 genomes	rs397509009
hgdp	rs397509009
ensembl	rs397509009
geneview	rs397509009
scholar	rs397509009
google	rs397509009
pharmgkb	rs397509009
gwascentral	rs397509009
openSNP	rs397509009
23andMe	rs397509009
SNPshot	rs397509009
SNPdbe	rs397509009
MSV3d	rs397509009
GWAS Ctlg	rs397509009

Status

Merged into rs80357942

Max Magnitude

0

ClinVar
Risk	rs397509009(A;A)
Alt	rs397509009(A;A)
Reference	Rs397509009(;)
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.41244799dupT
CLNSRC	Breast Cancer Information Core (BRCA1)
CLNACC	RCV000047957.2, RCV000111931.3,