rs1060502444

Orientation

plus

Stabilized

plus

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

Make rs1060502444(-;-)

Make rs1060502444(-;TC)

Make rs1060502444(TC;TC)

Reference

GRCh38.p7 38.3/150

Chromosome

13

Position

32340429

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs1060502444
dbSNP (classic)	rs1060502444
ClinGen	rs1060502444
ebi	rs1060502444
HLI	rs1060502444
Exac	rs1060502444
Gnomad	rs1060502444
Varsome	rs1060502444
LitVar	rs1060502444
Map	rs1060502444
PheGenI	rs1060502444
Biobank	rs1060502444
1000 genomes	rs1060502444
hgdp	rs1060502444
ensembl	rs1060502444
geneview	rs1060502444
scholar	rs1060502444
google	rs1060502444
pharmgkb	rs1060502444
gwascentral	rs1060502444
openSNP	rs1060502444
23andMe	rs1060502444
SNPshot	rs1060502444
SNPdbe	rs1060502444
MSV3d	rs1060502444
GWAS Ctlg	rs1060502444

Max Magnitude

0

ClinVar
Risk	rs1060502444(-;-)
Alt	rs1060502444(-;-)
Reference	Rs1060502444(CT;CT)
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.32914566_32914567delTC
CLNSRC
CLNACC	RCV000463421.1,