rs777371832

Orientation

plus

Stabilized

plus

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

Make rs777371832(AT;AT)

Reference

GRCh38.p7 38.3/149

Chromosome

17

Position

43091819

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs777371832
dbSNP (classic)	rs777371832
ClinGen	rs777371832
ebi	rs777371832
HLI	rs777371832
Exac	rs777371832
Gnomad	rs777371832
Varsome	rs777371832
LitVar	rs777371832
Map	rs777371832
PheGenI	rs777371832
Biobank	rs777371832
1000 genomes	rs777371832
hgdp	rs777371832
ensembl	rs777371832
geneview	rs777371832
scholar	rs777371832
google	rs777371832
pharmgkb	rs777371832
gwascentral	rs777371832
openSNP	rs777371832
23andMe	rs777371832
SNPshot	rs777371832
SNPdbe	rs777371832
MSV3d	rs777371832
GWAS Ctlg	rs777371832

Max Magnitude

6

aka c.788-791dupTA

ClinVar
Risk	rs777371832(TA;TA)
Alt	rs777371832(TA;TA)
Reference	Rs777371832(-;-)
Significance	Pathogenic
Disease	Breast-ovarian cancer
Variation	info
Gene	BRCA1
CLNDBN	Breast-ovarian cancer, familial 1
Reversed	0
HGVS	NC_000017.10:g.41243837_41243838dupTA
CLNSRC
CLNACC	RCV000240991.1,