rs276174897

plus

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

Make rs276174897(AG;AG)

Reference

GRCh38 38.1/142

Chromosome

13

Position

32362638

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs276174897
dbSNP (classic)	rs276174897
ClinGen	rs276174897
ebi	rs276174897
HLI	rs276174897
Exac	rs276174897
Gnomad	rs276174897
Varsome	rs276174897
LitVar	rs276174897
Map	rs276174897
PheGenI	rs276174897
Biobank	rs276174897
1000 genomes	rs276174897
hgdp	rs276174897
ensembl	rs276174897
geneview	rs276174897
scholar	rs276174897
google	rs276174897
pharmgkb	rs276174897
gwascentral	rs276174897
openSNP	rs276174897
23andMe	rs276174897
SNPshot	rs276174897
SNPdbe	rs276174897
MSV3d	rs276174897
GWAS Ctlg	rs276174897

Max Magnitude

6

rs276174897, also known as 8149del6insAG, c.7921_7926delinsAG and p.Glu2641_Phe2642?fs, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar.

ClinVar
Risk	rs276174897(AG;AG)
Alt	rs276174897(AG;AG)
Reference	Rs276174897(GAATTT;GAATTT)
Significance	Pathogenic
Disease	Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32936775_32936780delGAATTTinsAG
CLNSRC	Breast Cancer Information Core (BRCA2)
CLNACC	RCV000113839.2,