rs1060502459

Orientation

plus

Stabilized

plus

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

Make rs1060502459(A;A)

Make rs1060502459(A;T)

Reference

GRCh38.p7 38.3/150

Chromosome

13

Position

32362593

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs1060502459
dbSNP (classic)	rs1060502459
ClinGen	rs1060502459
ebi	rs1060502459
HLI	rs1060502459
Exac	rs1060502459
Gnomad	rs1060502459
Varsome	rs1060502459
LitVar	rs1060502459
Map	rs1060502459
PheGenI	rs1060502459
Biobank	rs1060502459
1000 genomes	rs1060502459
hgdp	rs1060502459
ensembl	rs1060502459
geneview	rs1060502459
scholar	rs1060502459
google	rs1060502459
pharmgkb	rs1060502459
gwascentral	rs1060502459
openSNP	rs1060502459
23andMe	rs1060502459
SNPshot	rs1060502459
SNPdbe	rs1060502459
MSV3d	rs1060502459
GWAS Ctlg	rs1060502459

Max Magnitude

0

ClinVar
Risk	rs1060502459(A;A)
Alt	rs1060502459(A;A)
Reference	Rs1060502459(T;T)
Significance	Probable-Pathogenic
Disease	Hereditary breast and ovarian cancer syndrome not provided
Variation	info
Gene	BRCA2
CLNDBN	Hereditary breast and ovarian cancer syndrome not provided
Reversed	0
HGVS	NC_000013.10:g.32936730T>A; NC_000013.10:g.32936730T>C
CLNSRC
CLNACC	RCV000465347.1, RCV000493105.1,