rs398122690

Orientation

minus

Stabilized

minus

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

Make rs398122690(G;G)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43063954

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs398122690
dbSNP (classic)	rs398122690
ClinGen	rs398122690
ebi	rs398122690
HLI	rs398122690
Exac	rs398122690
Gnomad	rs398122690
Varsome	rs398122690
LitVar	rs398122690
Map	rs398122690
PheGenI	rs398122690
Biobank	rs398122690
1000 genomes	rs398122690
hgdp	rs398122690
ensembl	rs398122690
geneview	rs398122690
scholar	rs398122690
google	rs398122690
pharmgkb	rs398122690
gwascentral	rs398122690
openSNP	rs398122690
23andMe	rs398122690
SNPshot	rs398122690
SNPdbe	rs398122690
MSV3d	rs398122690
GWAS Ctlg	rs398122690

Max Magnitude

0

ClinVar
Risk	rs398122690(G;G) rs398122690(T;T)
Alt	rs398122690(G;G) rs398122690(T;T)
Reference	Rs398122690(C;C)
Significance	Probable-Pathogenic
Disease	not specified Breast-ovarian cancer
Variation	info
Gene	BRCA1
CLNDBN	not specified Breast-ovarian cancer, familial 1
Reversed	1
HGVS	NC_000017.10:g.41215971G>A; NC_000017.10:g.41215971G>C
CLNSRC	ClinVar
CLNACC	RCV000421779.1, RCV000077154.2,