rs876658427

Orientation

plus

Stabilized

plus

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

Make rs876658427(-;-)

Make rs876658427(-;A)

Reference

GRCh38.p2 38.2/147

Chromosome

13

Position

32337751

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs876658427
dbSNP (classic)	rs876658427
ClinGen	rs876658427
ebi	rs876658427
HLI	rs876658427
Exac	rs876658427
Gnomad	rs876658427
Varsome	rs876658427
LitVar	rs876658427
Map	rs876658427
PheGenI	rs876658427
Biobank	rs876658427
1000 genomes	rs876658427
hgdp	rs876658427
ensembl	rs876658427
geneview	rs876658427
scholar	rs876658427
google	rs876658427
pharmgkb	rs876658427
gwascentral	rs876658427
openSNP	rs876658427
23andMe	rs876658427
SNPshot	rs876658427
SNPdbe	rs876658427
MSV3d	rs876658427
GWAS Ctlg	rs876658427

Max Magnitude

0

ClinVar
Risk	rs876658427(-;-)
Alt	rs876658427(-;-)
Reference	Rs876658427(A;A)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	BRCA2
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000013.10:g.32911888delA
CLNSRC
CLNACC	RCV000216535.1,