rs876661285

Orientation

plus

Stabilized

plus

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

Make rs876661285(-;-)

Make rs876661285(-;A)

Reference

GRCh38.p2 38.2/147

Chromosome

13

Position

32396984

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs876661285
dbSNP (classic)	rs876661285
ClinGen	rs876661285
ebi	rs876661285
HLI	rs876661285
Exac	rs876661285
Gnomad	rs876661285
Varsome	rs876661285
LitVar	rs876661285
Map	rs876661285
PheGenI	rs876661285
Biobank	rs876661285
1000 genomes	rs876661285
hgdp	rs876661285
ensembl	rs876661285
geneview	rs876661285
scholar	rs876661285
google	rs876661285
pharmgkb	rs876661285
gwascentral	rs876661285
openSNP	rs876661285
23andMe	rs876661285
SNPshot	rs876661285
SNPdbe	rs876661285
MSV3d	rs876661285
GWAS Ctlg	rs876661285

Max Magnitude

0

ClinVar
Risk	rs876661285(-;-)
Alt	rs876661285(-;-)
Reference	Rs876661285(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	BRCA2
CLNDBN	not provided
Reversed	0
HGVS	NC_000013.10:g.32971121delA
CLNSRC
CLNACC	RCV000217863.1,