rs876661270

Orientation

plus

Stabilized

plus

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

Make rs876661270(-;-)

Make rs876661270(-;CT)

Reference

GRCh38.p2 38.2/147

Chromosome

13

Position

32337414

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs876661270
dbSNP (classic)	rs876661270
ClinGen	rs876661270
ebi	rs876661270
HLI	rs876661270
Exac	rs876661270
Gnomad	rs876661270
Varsome	rs876661270
LitVar	rs876661270
Map	rs876661270
PheGenI	rs876661270
Biobank	rs876661270
1000 genomes	rs876661270
hgdp	rs876661270
ensembl	rs876661270
geneview	rs876661270
scholar	rs876661270
google	rs876661270
pharmgkb	rs876661270
gwascentral	rs876661270
openSNP	rs876661270
23andMe	rs876661270
SNPshot	rs876661270
SNPdbe	rs876661270
MSV3d	rs876661270
GWAS Ctlg	rs876661270

Max Magnitude

0

ClinVar
Risk	rs876661270(-;-)
Alt	rs876661270(-;-)
Reference	Rs876661270(CT;CT)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	BRCA2
CLNDBN	not provided
Reversed	0
HGVS	NC_000013.10:g.32911551_32911552delCT
CLNSRC
CLNACC	RCV000217537.1,