rs397509088

Merged into

rs80357512

Orientation

minus

Stabilized

minus

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

Make rs397509088(-;A)

Make rs397509088(A;A)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43091906

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397509088
dbSNP (classic)	rs397509088
ClinGen	rs397509088
ebi	rs397509088
HLI	rs397509088
Exac	rs397509088
Gnomad	rs397509088
Varsome	rs397509088
LitVar	rs397509088
Map	rs397509088
PheGenI	rs397509088
Biobank	rs397509088
1000 genomes	rs397509088
hgdp	rs397509088
ensembl	rs397509088
geneview	rs397509088
scholar	rs397509088
google	rs397509088
pharmgkb	rs397509088
gwascentral	rs397509088
openSNP	rs397509088
23andMe	rs397509088
SNPshot	rs397509088
SNPdbe	rs397509088
MSV3d	rs397509088
GWAS Ctlg	rs397509088

Status

Merged into rs80357512

Max Magnitude

0

ClinVar
Risk	rs397509088(A;A)
Alt	rs397509088(A;A)
Reference	Rs397509088(;)
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.41243924dupT
CLNSRC	Breast Cancer Information Core (BRCA1)
CLNACC	RCV000048259.2, RCV000112139.3,