rs397509276

Merged into

rs80357838

Orientation

minus

Stabilized

minus

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

Make rs397509276(-;T)

Make rs397509276(T;T)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43049140

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397509276
dbSNP (classic)	rs397509276
ClinGen	rs397509276
ebi	rs397509276
HLI	rs397509276
Exac	rs397509276
Gnomad	rs397509276
Varsome	rs397509276
LitVar	rs397509276
Map	rs397509276
PheGenI	rs397509276
Biobank	rs397509276
1000 genomes	rs397509276
hgdp	rs397509276
ensembl	rs397509276
geneview	rs397509276
scholar	rs397509276
google	rs397509276
pharmgkb	rs397509276
gwascentral	rs397509276
openSNP	rs397509276
23andMe	rs397509276
SNPshot	rs397509276
SNPdbe	rs397509276
MSV3d	rs397509276
GWAS Ctlg	rs397509276

Status

Merged into rs80357838

Max Magnitude

0

ClinVar
Risk	rs397509276(T;T)
Alt	rs397509276(T;T)
Reference	Rs397509276(;)
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.41201158dupA
CLNSRC	Breast Cancer Information Core (BRCA1)
CLNACC	RCV000048969.2, RCV000112631.2,