rs876658790

Orientation

minus

Stabilized

minus

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

Make rs876658790(A;A)

Make rs876658790(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

17

Position

43076615

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs876658790
dbSNP (classic)	rs876658790
ClinGen	rs876658790
ebi	rs876658790
HLI	rs876658790
Exac	rs876658790
Gnomad	rs876658790
Varsome	rs876658790
LitVar	rs876658790
Map	rs876658790
PheGenI	rs876658790
Biobank	rs876658790
1000 genomes	rs876658790
hgdp	rs876658790
ensembl	rs876658790
geneview	rs876658790
scholar	rs876658790
google	rs876658790
pharmgkb	rs876658790
gwascentral	rs876658790
openSNP	rs876658790
23andMe	rs876658790
SNPshot	rs876658790
SNPdbe	rs876658790
MSV3d	rs876658790
GWAS Ctlg	rs876658790

Max Magnitude

0

ClinVar
Risk	rs876658790(A;A)
Alt	rs876658790(A;A)
Reference	Rs876658790(G;G)
Significance	Probable-Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	BRCA1
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000017.10:g.41228632C>T
CLNSRC
CLNACC	RCV000216055.1,