rs397509208

Merged into

rs80357761

Orientation

minus

Stabilized

minus

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

Make rs397509208(-;-)

Make rs397509208(-;A)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43070969

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397509208
dbSNP (classic)	rs397509208
ClinGen	rs397509208
ebi	rs397509208
HLI	rs397509208
Exac	rs397509208
Gnomad	rs397509208
Varsome	rs397509208
LitVar	rs397509208
Map	rs397509208
PheGenI	rs397509208
Biobank	rs397509208
1000 genomes	rs397509208
hgdp	rs397509208
ensembl	rs397509208
geneview	rs397509208
scholar	rs397509208
google	rs397509208
pharmgkb	rs397509208
gwascentral	rs397509208
openSNP	rs397509208
23andMe	rs397509208
SNPshot	rs397509208
SNPdbe	rs397509208
MSV3d	rs397509208
GWAS Ctlg	rs397509208

Status

Merged into rs80357761

Max Magnitude

0

ClinVar
Risk
Alt
Reference	Rs397509208(A;A)
Significance	Pathogenic
Disease	Familial cancer of breast Breast-ovarian cancer not specified
Variation	info
Gene	BRCA1
CLNDBN	Familial cancer of breast Breast-ovarian cancer, familial 1 not specified
Reversed	1
HGVS	NC_000017.10:g.41222986delT
CLNSRC	Breast Cancer Information Core (BRCA1)
CLNACC	RCV000048705.2, RCV000112431.3, RCV000239002.1,