rs276174844

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;GTTTT)	1	Variant of uncertain significance in ClinVar
(GTTTT;GTTTT)	0	common in clinvar
(TTTGT;TTTGT)	0	common in clinvar

Make rs276174844(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32326089

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs276174844
dbSNP (classic)	rs276174844
ClinGen	rs276174844
ebi	rs276174844
HLI	rs276174844
Exac	rs276174844
Gnomad	rs276174844
Varsome	rs276174844
LitVar	rs276174844
Map	rs276174844
PheGenI	rs276174844
Biobank	rs276174844
1000 genomes	rs276174844
hgdp	rs276174844
ensembl	rs276174844
geneview	rs276174844
scholar	rs276174844
google	rs276174844
pharmgkb	rs276174844
gwascentral	rs276174844
openSNP	rs276174844
23andMe	rs276174844
SNPshot	rs276174844
SNPdbe	rs276174844
MSV3d	rs276174844
GWAS Ctlg	rs276174844

Max Magnitude

1

ClinVar
Risk	rs276174844(-;-)
Alt	rs276174844(-;-)
Reference	Rs276174844(TTTGT;TTTGT)
Significance	Probable-Pathogenic
Disease	not provided Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome
Variation	info
Gene	BRCA2
CLNDBN	not provided Breast-ovarian cancer, familial 2 Hereditary breast and ovarian cancer syndrome
Reversed	0
HGVS	NC_000013.10:g.32900226_32900230delGTTTT
CLNSRC	Breast Cancer Information Core (BRCA2)
CLNACC	RCV000044380.6, RCV000113566.1, RCV000203666.1,