rs397507205

Orientation

minus

Stabilized

minus

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

Make rs397507205(T;T)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43092666

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397507205
dbSNP (classic)	rs397507205
ClinGen	rs397507205
ebi	rs397507205
HLI	rs397507205
Exac	rs397507205
Gnomad	rs397507205
Varsome	rs397507205
LitVar	rs397507205
Map	rs397507205
PheGenI	rs397507205
Biobank	rs397507205
1000 genomes	rs397507205
hgdp	rs397507205
ensembl	rs397507205
geneview	rs397507205
scholar	rs397507205
google	rs397507205
pharmgkb	rs397507205
gwascentral	rs397507205
openSNP	rs397507205
23andMe	rs397507205
SNPshot	rs397507205
SNPdbe	rs397507205
MSV3d	rs397507205
GWAS Ctlg	rs397507205

Max Magnitude

6

ClinVar
Risk	rs397507205(T;T)
Alt	rs397507205(T;T)
Reference	Rs397507205(-;-)
Significance	Pathogenic
Disease	Breast-ovarian cancer
Variation	info
Gene	BRCA1
CLNDBN	Breast-ovarian cancer, familial 1
Reversed	1
HGVS	NC_000017.10:g.41244683_41244684insA
CLNSRC	ClinVar
CLNACC	RCV000031073.3,