rs398122636

Orientation

minus

Stabilized

minus

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

Make rs398122636(T;T)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43094018

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs398122636
dbSNP (classic)	rs398122636
ClinGen	rs398122636
ebi	rs398122636
HLI	rs398122636
Exac	rs398122636
Gnomad	rs398122636
Varsome	rs398122636
LitVar	rs398122636
Map	rs398122636
PheGenI	rs398122636
Biobank	rs398122636
1000 genomes	rs398122636
hgdp	rs398122636
ensembl	rs398122636
geneview	rs398122636
scholar	rs398122636
google	rs398122636
pharmgkb	rs398122636
gwascentral	rs398122636
openSNP	rs398122636
23andMe	rs398122636
SNPshot	rs398122636
SNPdbe	rs398122636
MSV3d	rs398122636
GWAS Ctlg	rs398122636

Max Magnitude

6

ClinVar
Risk	rs398122636(T;T)
Alt	rs398122636(T;T)
Reference	Rs398122636(-;-)
Significance	Pathogenic
Disease	Breast-ovarian cancer
Variation	info
Gene	BRCA1
CLNDBN	Breast-ovarian cancer, familial 1
Reversed	1
HGVS	NC_000017.10:g.41246036dupA
CLNSRC	ClinVar
CLNACC	RCV000077071.4,