rs606231392

Merged into

rs273898673

Orientation

minus

Stabilized

minus

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

Make rs606231392(A;A)

Reference

GRCh38.p2 38.2/144

Chromosome

17

Position

43106463

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs606231392
dbSNP (classic)	rs606231392
ClinGen	rs606231392
ebi	rs606231392
HLI	rs606231392
Exac	rs606231392
Gnomad	rs606231392
Varsome	rs606231392
LitVar	rs606231392
Map	rs606231392
PheGenI	rs606231392
Biobank	rs606231392
1000 genomes	rs606231392
hgdp	rs606231392
ensembl	rs606231392
geneview	rs606231392
scholar	rs606231392
google	rs606231392
pharmgkb	rs606231392
gwascentral	rs606231392
openSNP	rs606231392
23andMe	rs606231392
SNPshot	rs606231392
SNPdbe	rs606231392
MSV3d	rs606231392
GWAS Ctlg	rs606231392

Status

Merged into rs273898673

Max Magnitude

6

ClinVar
Risk	rs606231392(A;A)
Alt	rs606231392(A;A)
Reference	Rs606231392(;)
Significance	Pathogenic
Disease	Breast-ovarian cancer
Variation	info
Gene	BRCA1
CLNDBN	Breast-ovarian cancer, familial 1
Reversed	1
HGVS	NC_000017.10:g.41258481dupT
CLNSRC	Breast Cancer Information Core (BRCA1)
CLNACC	RCV000112003.1,