rs397509280

Orientation

minus

Stabilized

minus

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

Make rs397509280(A;G)

Make rs397509280(G;G)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43049114

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397509280
dbSNP (classic)	rs397509280
ClinGen	rs397509280
ebi	rs397509280
HLI	rs397509280
Exac	rs397509280
Gnomad	rs397509280
Varsome	rs397509280
LitVar	rs397509280
Map	rs397509280
PheGenI	rs397509280
Biobank	rs397509280
1000 genomes	rs397509280
hgdp	rs397509280
ensembl	rs397509280
geneview	rs397509280
scholar	rs397509280
google	rs397509280
pharmgkb	rs397509280
gwascentral	rs397509280
openSNP	rs397509280
23andMe	rs397509280
SNPshot	rs397509280
SNPdbe	rs397509280
MSV3d	rs397509280
GWAS Ctlg	rs397509280

Max Magnitude

0

ClinVar
Risk	rs397509280(G;G)
Alt	rs397509280(G;G)
Reference	Rs397509280(A;A)
Significance	Probable-non-pathogenic
Disease	Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer not specified
Variation	info
Gene	BRCA1
CLNDBN	Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 1 not specified
Reversed	1
HGVS	NC_000017.10:g.41201131T>C
CLNSRC	ClinVar
CLNACC	RCV000048979.3, RCV000077622.3, RCV000433814.1,