rs397509311

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(-;TC)	6	BRCA1 variant considered pathogenic for breast cancer
(TC;TC)	0	common in clinvar

Make rs397509311(-;-)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43124024

Gene	BRCA1, NBR2

is a	snp
is	mentioned by
dbSNP	rs397509311
dbSNP (classic)	rs397509311
ClinGen	rs397509311
ebi	rs397509311
HLI	rs397509311
Exac	rs397509311
Gnomad	rs397509311
Varsome	rs397509311
LitVar	rs397509311
Map	rs397509311
PheGenI	rs397509311
Biobank	rs397509311
1000 genomes	rs397509311
hgdp	rs397509311
ensembl	rs397509311
geneview	rs397509311
scholar	rs397509311
google	rs397509311
pharmgkb	rs397509311
gwascentral	rs397509311
openSNP	rs397509311
23andMe	rs397509311
SNPshot	rs397509311
SNPdbe	rs397509311
MSV3d	rs397509311
GWAS Ctlg	rs397509311

Max Magnitude

6

aka c.-16_-15del

ClinVar
Risk	rs397509311(-;-)
Alt	rs397509311(-;-)
Reference	Rs397509311(TC;TC)
Significance	Untested
Disease	Familial cancer of breast
Variation	info
Gene	NBR2 BRCA1
CLNDBN	Familial cancer of breast
Reversed	1
HGVS	NC_000017.10:g.41276041_41276042delGA
CLNSRC	ClinVar
CLNACC	RCV000049110.2,