rs1060502414

Orientation

plus

Stabilized

plus

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

Make rs1060502414(C;T)

Make rs1060502414(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

13

Position

32336945

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs1060502414
dbSNP (classic)	rs1060502414
ClinGen	rs1060502414
ebi	rs1060502414
HLI	rs1060502414
Exac	rs1060502414
Gnomad	rs1060502414
Varsome	rs1060502414
LitVar	rs1060502414
Map	rs1060502414
PheGenI	rs1060502414
Biobank	rs1060502414
1000 genomes	rs1060502414
hgdp	rs1060502414
ensembl	rs1060502414
geneview	rs1060502414
scholar	rs1060502414
google	rs1060502414
pharmgkb	rs1060502414
gwascentral	rs1060502414
openSNP	rs1060502414
23andMe	rs1060502414
SNPshot	rs1060502414
SNPdbe	rs1060502414
MSV3d	rs1060502414
GWAS Ctlg	rs1060502414

Max Magnitude

0

ClinVar
Risk	rs1060502414(T;T)
Alt	rs1060502414(T;T)
Reference	Rs1060502414(C;C)
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.32911082C>T
CLNSRC
CLNACC	RCV000461340.1,