rs876659830

Orientation

minus

Stabilized

minus

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

Make rs876659830(-;-)

Make rs876659830(-;C)

Reference

GRCh38.p2 38.2/147

Chromosome

17

Position

43099866

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs876659830
dbSNP (classic)	rs876659830
ClinGen	rs876659830
ebi	rs876659830
HLI	rs876659830
Exac	rs876659830
Gnomad	rs876659830
Varsome	rs876659830
LitVar	rs876659830
Map	rs876659830
PheGenI	rs876659830
Biobank	rs876659830
1000 genomes	rs876659830
hgdp	rs876659830
ensembl	rs876659830
geneview	rs876659830
scholar	rs876659830
google	rs876659830
pharmgkb	rs876659830
gwascentral	rs876659830
openSNP	rs876659830
23andMe	rs876659830
SNPshot	rs876659830
SNPdbe	rs876659830
MSV3d	rs876659830
GWAS Ctlg	rs876659830

Max Magnitude

0

ClinVar
Risk	rs876659830(-;-)
Alt	rs876659830(-;-)
Reference	Rs876659830(C;C)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	BRCA1
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000017.10:g.41251883delG
CLNSRC
CLNACC	RCV000221805.1,