rs876659318

Orientation

plus

Stabilized

plus

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

Make rs876659318(-;-)

Make rs876659318(-;C)

Reference

GRCh38.p2 38.2/147

Chromosome

13

Position

32336611

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs876659318
dbSNP (classic)	rs876659318
ClinGen	rs876659318
ebi	rs876659318
HLI	rs876659318
Exac	rs876659318
Gnomad	rs876659318
Varsome	rs876659318
LitVar	rs876659318
Map	rs876659318
PheGenI	rs876659318
Biobank	rs876659318
1000 genomes	rs876659318
hgdp	rs876659318
ensembl	rs876659318
geneview	rs876659318
scholar	rs876659318
google	rs876659318
pharmgkb	rs876659318
gwascentral	rs876659318
openSNP	rs876659318
23andMe	rs876659318
SNPshot	rs876659318
SNPdbe	rs876659318
MSV3d	rs876659318
GWAS Ctlg	rs876659318

Max Magnitude

0

ClinVar
Risk	rs876659318(-;-)
Alt	rs876659318(-;-)
Reference	Rs876659318(C;C)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	BRCA2
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000013.10:g.32910748delC
CLNSRC
CLNACC	RCV000220476.1,