rs431825413

Merged into

rs80357906

Orientation

minus

Stabilized

minus

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

Make rs431825413(-;C)

Make rs431825413(C;C)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43057064

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs431825413
dbSNP (classic)	rs431825413
ClinGen	rs431825413
ebi	rs431825413
HLI	rs431825413
Exac	rs431825413
Gnomad	rs431825413
Varsome	rs431825413
LitVar	rs431825413
Map	rs431825413
PheGenI	rs431825413
Biobank	rs431825413
1000 genomes	rs431825413
hgdp	rs431825413
ensembl	rs431825413
geneview	rs431825413
scholar	rs431825413
google	rs431825413
pharmgkb	rs431825413
gwascentral	rs431825413
openSNP	rs431825413
23andMe	rs431825413
SNPshot	rs431825413
SNPdbe	rs431825413
MSV3d	rs431825413
GWAS Ctlg	rs431825413

Status

Merged into rs80357906

Max Magnitude

0

ClinVar
Risk	rs431825413(C;C)
Alt	rs431825413(C;C)
Reference	Rs431825413(;)
Significance	Other
Disease	Breast-ovarian cancer Pancreatic cancer Familial cancer of breast Hereditary breast and ovarian cancer syndrome Hereditary cancer-predisposing syndrome
Variation	info
Gene	BRCA1
CLNDBN	Breast-ovarian cancer, familial 1 Pancreatic cancer, susceptibility to Familial cancer of breast Hereditary breast and ovarian cancer syndrome Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000017.10:g.41209082dupG
CLNSRC	Breast Cancer Information Core (BRCA1) Inc. OMIM Allelic Variant
CLNACC	RCV000019246.18, RCV000019247.3, RCV000056287.6, RCV000119097.6, RCV000131328.4,