rs876659229

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(GATA;GATA)	0	common in clinvar

Make rs876659229(-;-)

Make rs876659229(-;AGAT)

Make rs876659229(AGAT;AGAT)

Reference

GRCh38.p2 38.2/147

Chromosome

13

Position

32356426

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs876659229
dbSNP (classic)	rs876659229
ClinGen	rs876659229
ebi	rs876659229
HLI	rs876659229
Exac	rs876659229
Gnomad	rs876659229
Varsome	rs876659229
LitVar	rs876659229
Map	rs876659229
PheGenI	rs876659229
Biobank	rs876659229
1000 genomes	rs876659229
hgdp	rs876659229
ensembl	rs876659229
geneview	rs876659229
scholar	rs876659229
google	rs876659229
pharmgkb	rs876659229
gwascentral	rs876659229
openSNP	rs876659229
23andMe	rs876659229
SNPshot	rs876659229
SNPdbe	rs876659229
MSV3d	rs876659229
GWAS Ctlg	rs876659229

Max Magnitude

0

ClinVar
Risk	rs876659229(-;-)
Alt	rs876659229(-;-)
Reference	Rs876659229(GATA;GATA)
Significance	Probable-Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	BRCA2
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000013.10:g.32930563_32930566delAGAT
CLNSRC
CLNACC	RCV000215010.1,