rs876659047

Orientation

plus

Stabilized

plus

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

Make rs876659047(AT;AT)

Make rs876659047(AT;TC)

Reference

GRCh38.p2 38.2/147

Chromosome

13

Position

32380084

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs876659047
dbSNP (classic)	rs876659047
ClinGen	rs876659047
ebi	rs876659047
HLI	rs876659047
Exac	rs876659047
Gnomad	rs876659047
Varsome	rs876659047
LitVar	rs876659047
Map	rs876659047
PheGenI	rs876659047
Biobank	rs876659047
1000 genomes	rs876659047
hgdp	rs876659047
ensembl	rs876659047
geneview	rs876659047
scholar	rs876659047
google	rs876659047
pharmgkb	rs876659047
gwascentral	rs876659047
openSNP	rs876659047
23andMe	rs876659047
SNPshot	rs876659047
SNPdbe	rs876659047
MSV3d	rs876659047
GWAS Ctlg	rs876659047

Max Magnitude

0

ClinVar
Risk	rs876659047(AT;AT)
Alt	rs876659047(AT;AT)
Reference	Rs876659047(TC;TC)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32954221_32954222delTCinsAT
CLNSRC
CLNACC	RCV000215926.1, RCV000229620.2, RCV000411658.1,