rs587781526

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(TCTATGATCTCTTTAGGGGT;TCTATGATCTCTTTAGGGGT)	0	common in clinvar

Make rs587781526(AATA;AATA)

Make rs587781526(AATA;TCTATGATCTCTTTAGGGGT)

Reference

GRCh38.p2 38.2/144

Chromosome

17

Position

43063370

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs587781526
dbSNP (classic)	rs587781526
ClinGen	rs587781526
ebi	rs587781526
HLI	rs587781526
Exac	rs587781526
Gnomad	rs587781526
Varsome	rs587781526
LitVar	rs587781526
Map	rs587781526
PheGenI	rs587781526
Biobank	rs587781526
1000 genomes	rs587781526
hgdp	rs587781526
ensembl	rs587781526
geneview	rs587781526
scholar	rs587781526
google	rs587781526
pharmgkb	rs587781526
gwascentral	rs587781526
openSNP	rs587781526
23andMe	rs587781526
SNPshot	rs587781526
SNPdbe	rs587781526
MSV3d	rs587781526
GWAS Ctlg	rs587781526

Max Magnitude

0

ClinVar
Risk	rs587781526(AATA;AATA)
Alt	rs587781526(AATA;AATA)
Reference	Rs587781526(TCTATGATCTCTTTAGGGGT;TCTATGATCTCTTTAGGGGT)
Significance	Probable-Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	BRCA1
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000017.10:g.41215387_41215406del20insTATT
CLNSRC
CLNACC	RCV000129518.1,