rs863224466

Merged into

rs397507785

Orientation

plus

Stabilized

plus

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

Make rs863224466(-;-)

Make rs863224466(-;T)

Reference

GRCh38.p2 38.2/146

Chromosome

13

Position

32339793

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs863224466
dbSNP (classic)	rs863224466
ClinGen	rs863224466
ebi	rs863224466
HLI	rs863224466
Exac	rs863224466
Gnomad	rs863224466
Varsome	rs863224466
LitVar	rs863224466
Map	rs863224466
PheGenI	rs863224466
Biobank	rs863224466
1000 genomes	rs863224466
hgdp	rs863224466
ensembl	rs863224466
geneview	rs863224466
scholar	rs863224466
google	rs863224466
pharmgkb	rs863224466
gwascentral	rs863224466
openSNP	rs863224466
23andMe	rs863224466
SNPshot	rs863224466
SNPdbe	rs863224466
MSV3d	rs863224466
GWAS Ctlg	rs863224466

Status

Merged into rs397507785

Max Magnitude

0

ClinVar
Risk
Alt
Reference	Rs863224466(T;T)
Significance	Pathogenic
Disease	Familial cancer of breast Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32913931delT
CLNSRC
CLNACC	RCV000044661.2, RCV000198909.1, RCV000241279.1,