rs876660541

Orientation

plus

Stabilized

plus

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

Make rs876660541(TTTT;TTTT)

Reference

GRCh38.p2 38.2/147

Chromosome

13

Position

32341057

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs876660541
dbSNP (classic)	rs876660541
ClinGen	rs876660541
ebi	rs876660541
HLI	rs876660541
Exac	rs876660541
Gnomad	rs876660541
Varsome	rs876660541
LitVar	rs876660541
Map	rs876660541
PheGenI	rs876660541
Biobank	rs876660541
1000 genomes	rs876660541
hgdp	rs876660541
ensembl	rs876660541
geneview	rs876660541
scholar	rs876660541
google	rs876660541
pharmgkb	rs876660541
gwascentral	rs876660541
openSNP	rs876660541
23andMe	rs876660541
SNPshot	rs876660541
SNPdbe	rs876660541
MSV3d	rs876660541
GWAS Ctlg	rs876660541

Max Magnitude

6

aka c.6699_6702dupTTTT; however, rs876660541 has been merged into rs587781516

ClinVar
Risk	rs876660541(TTTT;TTTT)
Alt	rs876660541(TTTT;TTTT)
Reference	Rs876660541(-;-)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	BRCA2
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000013.10:g.32915191_32915194dupTTTT
CLNSRC
CLNACC	RCV000215061.1,