rs397508861

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(-;A)	6	BRCA1 variant considered pathogenic for breast cancer
(A;A)	0	common in clinvar

Make rs397508861(-;-)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43094160

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397508861
dbSNP (classic)	rs397508861
ClinGen	rs397508861
ebi	rs397508861
HLI	rs397508861
Exac	rs397508861
Gnomad	rs397508861
Varsome	rs397508861
LitVar	rs397508861
Map	rs397508861
PheGenI	rs397508861
Biobank	rs397508861
1000 genomes	rs397508861
hgdp	rs397508861
ensembl	rs397508861
geneview	rs397508861
scholar	rs397508861
google	rs397508861
pharmgkb	rs397508861
gwascentral	rs397508861
openSNP	rs397508861
23andMe	rs397508861
SNPshot	rs397508861
SNPdbe	rs397508861
MSV3d	rs397508861
GWAS Ctlg	rs397508861

Max Magnitude

6

ClinVar
Risk	rs397508861(-;-)
Alt	rs397508861(-;-)
Reference	Rs397508861(A;A)
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.41246177delT
CLNSRC	ClinVar
CLNACC	RCV000047444.2, RCV000256751.2,