rs606231395

Merged into

rs80357838

Orientation

minus

Stabilized

minus

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

Make rs606231395(-;T)

Make rs606231395(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

17

Position

43049142

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs606231395
dbSNP (classic)	rs606231395
ClinGen	rs606231395
ebi	rs606231395
HLI	rs606231395
Exac	rs606231395
Gnomad	rs606231395
Varsome	rs606231395
LitVar	rs606231395
Map	rs606231395
PheGenI	rs606231395
Biobank	rs606231395
1000 genomes	rs606231395
hgdp	rs606231395
ensembl	rs606231395
geneview	rs606231395
scholar	rs606231395
google	rs606231395
pharmgkb	rs606231395
gwascentral	rs606231395
openSNP	rs606231395
23andMe	rs606231395
SNPshot	rs606231395
SNPdbe	rs606231395
MSV3d	rs606231395
GWAS Ctlg	rs606231395

Status

Merged into rs80357838

Max Magnitude

0

ClinVar
Risk	rs606231395(T;T)
Alt	rs606231395(T;T)
Reference	Rs606231395(;)
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.41201158dupA
CLNSRC	Breast Cancer Information Core (BRCA1)
CLNACC	RCV000048969.2, RCV000112631.2,