rs876659865

Orientation

minus

Stabilized

minus

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

Make rs876659865(-;AACA)

Make rs876659865(AACA;AACA)

Reference

GRCh38.p2 38.2/147

Chromosome

17

Position

43091596

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs876659865
dbSNP (classic)	rs876659865
ClinGen	rs876659865
ebi	rs876659865
HLI	rs876659865
Exac	rs876659865
Gnomad	rs876659865
Varsome	rs876659865
LitVar	rs876659865
Map	rs876659865
PheGenI	rs876659865
Biobank	rs876659865
1000 genomes	rs876659865
hgdp	rs876659865
ensembl	rs876659865
geneview	rs876659865
scholar	rs876659865
google	rs876659865
pharmgkb	rs876659865
gwascentral	rs876659865
openSNP	rs876659865
23andMe	rs876659865
SNPshot	rs876659865
SNPdbe	rs876659865
MSV3d	rs876659865
GWAS Ctlg	rs876659865

Max Magnitude

0

ClinVar
Risk	rs876659865(AACA;AACA)
Alt	rs876659865(AACA;AACA)
Reference	Rs876659865(-;-)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	BRCA1
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000017.10:g.41243614_41243617dupTGTT
CLNSRC
CLNACC	RCV000219345.1,