rs876659317

Orientation

plus

Stabilized

plus

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

Make rs876659317(-;GT)

Make rs876659317(GT;GT)

Reference

GRCh38.p2 38.2/147

Chromosome

13

Position

32326127

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs876659317
dbSNP (classic)	rs876659317
ClinGen	rs876659317
ebi	rs876659317
HLI	rs876659317
Exac	rs876659317
Gnomad	rs876659317
Varsome	rs876659317
LitVar	rs876659317
Map	rs876659317
PheGenI	rs876659317
Biobank	rs876659317
1000 genomes	rs876659317
hgdp	rs876659317
ensembl	rs876659317
geneview	rs876659317
scholar	rs876659317
google	rs876659317
pharmgkb	rs876659317
gwascentral	rs876659317
openSNP	rs876659317
23andMe	rs876659317
SNPshot	rs876659317
SNPdbe	rs876659317
MSV3d	rs876659317
GWAS Ctlg	rs876659317

Max Magnitude

0

ClinVar
Risk	rs876659317(TG;TG)
Alt	rs876659317(TG;TG)
Reference	Rs876659317(-;-)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	BRCA2
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000013.10:g.32900263_32900264dupGT
CLNSRC
CLNACC	RCV000219448.1,