rs397509042

Orientation

minus

Stabilized

minus

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

Make rs397509042(G;G)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43092373

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397509042
dbSNP (classic)	rs397509042
ClinGen	rs397509042
ebi	rs397509042
HLI	rs397509042
Exac	rs397509042
Gnomad	rs397509042
Varsome	rs397509042
LitVar	rs397509042
Map	rs397509042
PheGenI	rs397509042
Biobank	rs397509042
1000 genomes	rs397509042
hgdp	rs397509042
ensembl	rs397509042
geneview	rs397509042
scholar	rs397509042
google	rs397509042
pharmgkb	rs397509042
gwascentral	rs397509042
openSNP	rs397509042
23andMe	rs397509042
SNPshot	rs397509042
SNPdbe	rs397509042
MSV3d	rs397509042
GWAS Ctlg	rs397509042

Max Magnitude

6

aka c.788-1342dup

ClinVar
Risk	rs397509042(G;G)
Alt	rs397509042(G;G)
Reference	Rs397509042(-;-)
Significance	Untested
Disease	Familial cancer of breast
Variation	info
Gene	BRCA1
CLNDBN	Familial cancer of breast
Reversed	1
HGVS	NC_000017.10:g.41244391dupC
CLNSRC	ClinVar
CLNACC	RCV000048087.2,