rs398122555

Orientation

plus

Stabilized

plus

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

Make rs398122555(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32340747

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs398122555
dbSNP (classic)	rs398122555
ClinGen	rs398122555
ebi	rs398122555
HLI	rs398122555
Exac	rs398122555
Gnomad	rs398122555
Varsome	rs398122555
LitVar	rs398122555
Map	rs398122555
PheGenI	rs398122555
Biobank	rs398122555
1000 genomes	rs398122555
hgdp	rs398122555
ensembl	rs398122555
geneview	rs398122555
scholar	rs398122555
google	rs398122555
pharmgkb	rs398122555
gwascentral	rs398122555
openSNP	rs398122555
23andMe	rs398122555
SNPshot	rs398122555
SNPdbe	rs398122555
MSV3d	rs398122555
GWAS Ctlg	rs398122555

Max Magnitude

6

ClinVar
Risk	rs398122555(-;-)
Alt	rs398122555(-;-)
Reference	Rs398122555(TTAAA;TTAAA)
Significance	Pathogenic
Disease	Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32914884_32914888delAATTA
CLNSRC	ClinVar
CLNACC	RCV000076964.4,