rs606231394

Merged into

rs80357886

Orientation

minus

Stabilized

minus

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

Make rs606231394(-;G)

Make rs606231394(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

17

Position

43051108

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs606231394
dbSNP (classic)	rs606231394
ClinGen	rs606231394
ebi	rs606231394
HLI	rs606231394
Exac	rs606231394
Gnomad	rs606231394
Varsome	rs606231394
LitVar	rs606231394
Map	rs606231394
PheGenI	rs606231394
Biobank	rs606231394
1000 genomes	rs606231394
hgdp	rs606231394
ensembl	rs606231394
geneview	rs606231394
scholar	rs606231394
google	rs606231394
pharmgkb	rs606231394
gwascentral	rs606231394
openSNP	rs606231394
23andMe	rs606231394
SNPshot	rs606231394
SNPdbe	rs606231394
MSV3d	rs606231394
GWAS Ctlg	rs606231394

Status

Merged into rs80357886

Max Magnitude

0

ClinVar
Risk	rs606231394(G;G)
Alt	rs606231394(G;G)
Reference	Rs606231394(;)
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.41203123dupC
CLNSRC	Breast Cancer Information Core (BRCA1)
CLNACC	RCV000048912.2, RCV000112602.3,