rs397509225

Merged into

rs80358345

Orientation

minus

Stabilized

minus

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

Make rs397509225(-;-)

Make rs397509225(-;CTG)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43063946

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397509225
dbSNP (classic)	rs397509225
ClinGen	rs397509225
ebi	rs397509225
HLI	rs397509225
Exac	rs397509225
Gnomad	rs397509225
Varsome	rs397509225
LitVar	rs397509225
Map	rs397509225
PheGenI	rs397509225
Biobank	rs397509225
1000 genomes	rs397509225
hgdp	rs397509225
ensembl	rs397509225
geneview	rs397509225
scholar	rs397509225
google	rs397509225
pharmgkb	rs397509225
gwascentral	rs397509225
openSNP	rs397509225
23andMe	rs397509225
SNPshot	rs397509225
SNPdbe	rs397509225
MSV3d	rs397509225
GWAS Ctlg	rs397509225

Status

Merged into rs80358345

Max Magnitude

0

ClinVar
Risk
Alt
Reference	Rs397509225(CTG;CTG)
Significance	Other
Disease	Familial cancer of breast Breast-ovarian cancer Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	BRCA1
CLNDBN	Familial cancer of breast Breast-ovarian cancer, familial 1 Hereditary cancer-predisposing syndrome not provided
Reversed	1
HGVS	NC_000017.10:g.41215963_41215965delCAG
CLNSRC	ClinVar
CLNACC	RCV000048779.2, RCV000083215.3, RCV000166817.1, RCV000237025.1,