rs1060502395

Orientation

plus

Stabilized

plus

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

Make rs1060502395(-;-)

Make rs1060502395(-;G)

Reference

GRCh38.p7 38.3/150

Chromosome

13

Position

32326146

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs1060502395
dbSNP (classic)	rs1060502395
ClinGen	rs1060502395
ebi	rs1060502395
HLI	rs1060502395
Exac	rs1060502395
Gnomad	rs1060502395
Varsome	rs1060502395
LitVar	rs1060502395
Map	rs1060502395
PheGenI	rs1060502395
Biobank	rs1060502395
1000 genomes	rs1060502395
hgdp	rs1060502395
ensembl	rs1060502395
geneview	rs1060502395
scholar	rs1060502395
google	rs1060502395
pharmgkb	rs1060502395
gwascentral	rs1060502395
openSNP	rs1060502395
23andMe	rs1060502395
SNPshot	rs1060502395
SNPdbe	rs1060502395
MSV3d	rs1060502395
GWAS Ctlg	rs1060502395

Max Magnitude

0

ClinVar
Risk	rs1060502395(-;-)
Alt	rs1060502395(-;-)
Reference	Rs1060502395(G;G)
Significance	Pathogenic
Disease	Hereditary breast and ovarian cancer syndrome
Variation	info
Gene	BRCA2
CLNDBN	Hereditary breast and ovarian cancer syndrome
Reversed	0
HGVS	NC_000013.10:g.32900283delG
CLNSRC
CLNACC	RCV000461133.1,