rs876660623

Orientation

minus

Stabilized

minus

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

Make rs876660623(-;-)

Make rs876660623(-;G)

Reference

GRCh38.p2 38.2/147

Chromosome

17

Position

43094279

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs876660623
dbSNP (classic)	rs876660623
ClinGen	rs876660623
ebi	rs876660623
HLI	rs876660623
Exac	rs876660623
Gnomad	rs876660623
Varsome	rs876660623
LitVar	rs876660623
Map	rs876660623
PheGenI	rs876660623
Biobank	rs876660623
1000 genomes	rs876660623
hgdp	rs876660623
ensembl	rs876660623
geneview	rs876660623
scholar	rs876660623
google	rs876660623
pharmgkb	rs876660623
gwascentral	rs876660623
openSNP	rs876660623
23andMe	rs876660623
SNPshot	rs876660623
SNPdbe	rs876660623
MSV3d	rs876660623
GWAS Ctlg	rs876660623

Max Magnitude

0

ClinVar
Risk	rs876660623(-;-)
Alt	rs876660623(-;-)
Reference	Rs876660623(G;G)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	BRCA1
CLNDBN	Hereditary cancer-predisposing syndrome not provided
Reversed	1
HGVS	NC_000017.10:g.41246296delC
CLNSRC
CLNACC	RCV000218101.1, RCV000484830.1,