rs276174811

plus

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

Make rs276174811(T;T)

Reference

GRCh38 38.1/142

Chromosome

13

Position

32333085

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs276174811
dbSNP (classic)	rs276174811
ClinGen	rs276174811
ebi	rs276174811
HLI	rs276174811
Exac	rs276174811
Gnomad	rs276174811
Varsome	rs276174811
LitVar	rs276174811
Map	rs276174811
PheGenI	rs276174811
Biobank	rs276174811
1000 genomes	rs276174811
hgdp	rs276174811
ensembl	rs276174811
geneview	rs276174811
scholar	rs276174811
google	rs276174811
pharmgkb	rs276174811
gwascentral	rs276174811
openSNP	rs276174811
23andMe	rs276174811
SNPshot	rs276174811
SNPdbe	rs276174811
MSV3d	rs276174811
GWAS Ctlg	rs276174811

Merged from

Rs606231397

Max Magnitude

6

rs276174811, also known as 1835insT, c.1607_1608insT and p.Ser536?fs, is a variant in the BRCA2 gene considered pathogenic for breast cancer in ClinVar.

ClinVar
Risk	rs276174811(T;T)
Alt	rs276174811(T;T)
Reference	Rs276174811(-;-)
Significance	Pathogenic
Disease	Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32907223dupT
CLNSRC	Breast Cancer Information Core (BRCA2)
CLNACC	RCV000112942.2,