rs397509001

Merged into

rs80357899

Orientation

minus

Stabilized

minus

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

Make rs397509001(-;-)

Make rs397509001(-;TT)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43092828

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397509001
dbSNP (classic)	rs397509001
ClinGen	rs397509001
ebi	rs397509001
HLI	rs397509001
Exac	rs397509001
Gnomad	rs397509001
Varsome	rs397509001
LitVar	rs397509001
Map	rs397509001
PheGenI	rs397509001
Biobank	rs397509001
1000 genomes	rs397509001
hgdp	rs397509001
ensembl	rs397509001
geneview	rs397509001
scholar	rs397509001
google	rs397509001
pharmgkb	rs397509001
gwascentral	rs397509001
openSNP	rs397509001
23andMe	rs397509001
SNPshot	rs397509001
SNPdbe	rs397509001
MSV3d	rs397509001
GWAS Ctlg	rs397509001

Status

Merged into rs80357899

Max Magnitude

0

ClinVar
Risk
Alt
Reference	Rs397509001(TT;TT)
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.41244845_41244846delAA
CLNSRC	Breast Cancer Information Core (BRCA1)
CLNACC	RCV000047938.2, RCV000111921.3,