rs397509235

Orientation

minus

Stabilized

minus

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

Make rs397509235(-;-)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43063344

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397509235
dbSNP (classic)	rs397509235
ClinGen	rs397509235
ebi	rs397509235
HLI	rs397509235
Exac	rs397509235
Gnomad	rs397509235
Varsome	rs397509235
LitVar	rs397509235
Map	rs397509235
PheGenI	rs397509235
Biobank	rs397509235
1000 genomes	rs397509235
hgdp	rs397509235
ensembl	rs397509235
geneview	rs397509235
scholar	rs397509235
google	rs397509235
pharmgkb	rs397509235
gwascentral	rs397509235
openSNP	rs397509235
23andMe	rs397509235
SNPshot	rs397509235
SNPdbe	rs397509235
MSV3d	rs397509235
GWAS Ctlg	rs397509235

Max Magnitude

6

rs397509235 has merged into rs34570933

ClinVar
Risk	rs397509235(-;-)
Alt	rs397509235(-;-)
Reference	Rs397509235(A;A)
Significance	Untested
Disease	Familial cancer of breast
Variation	info
Gene	BRCA1
CLNDBN	Familial cancer of breast
Reversed	1
HGVS	NC_000017.10:g.41215361delT
CLNSRC	ClinVar
CLNACC	RCV000048846.2,