rs876660287

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;-)	0	common in clinvar
(-;AT)	6	BRCA2 variant considered pathogenic for breast cancer

Make rs876660287(AT;AT)

Reference

GRCh38.p2 38.2/147

Chromosome

13

Position

32398230

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs876660287
dbSNP (classic)	rs876660287
ClinGen	rs876660287
ebi	rs876660287
HLI	rs876660287
Exac	rs876660287
Gnomad	rs876660287
Varsome	rs876660287
LitVar	rs876660287
Map	rs876660287
PheGenI	rs876660287
Biobank	rs876660287
1000 genomes	rs876660287
hgdp	rs876660287
ensembl	rs876660287
geneview	rs876660287
scholar	rs876660287
google	rs876660287
pharmgkb	rs876660287
gwascentral	rs876660287
openSNP	rs876660287
23andMe	rs876660287
SNPshot	rs876660287
SNPdbe	rs876660287
MSV3d	rs876660287
GWAS Ctlg	rs876660287

Max Magnitude

6

aka c.9717_9718insAT

ClinVar
Risk	rs876660287(TA;TA)
Alt	rs876660287(TA;TA)
Reference	Rs876660287(-;-)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	BRCA2
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000013.10:g.32972367_32972368insAT
CLNSRC
CLNACC	RCV000218421.1,