rs878853577

Orientation

plus

Stabilized

plus

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

Make rs878853577(-;CATC)

Make rs878853577(CATC;CATC)

Reference

GRCh38.p2 38.2/147

Chromosome

13

Position

32338362

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs878853577
dbSNP (classic)	rs878853577
ClinGen	rs878853577
ebi	rs878853577
HLI	rs878853577
Exac	rs878853577
Gnomad	rs878853577
Varsome	rs878853577
LitVar	rs878853577
Map	rs878853577
PheGenI	rs878853577
Biobank	rs878853577
1000 genomes	rs878853577
hgdp	rs878853577
ensembl	rs878853577
geneview	rs878853577
scholar	rs878853577
google	rs878853577
pharmgkb	rs878853577
gwascentral	rs878853577
openSNP	rs878853577
23andMe	rs878853577
SNPshot	rs878853577
SNPdbe	rs878853577
MSV3d	rs878853577
GWAS Ctlg	rs878853577

Max Magnitude

0

ClinVar
Risk	rs878853577(CATC;CATC)
Alt	rs878853577(CATC;CATC)
Reference	Rs878853577(-;-)
Significance	Pathogenic
Disease	Hereditary breast and ovarian cancer syndrome
Variation	info
Gene	BRCA2
CLNDBN	Hereditary breast and ovarian cancer syndrome
Reversed	0
HGVS	NC_000013.10:g.32912499_32912500insCATC
CLNSRC
CLNACC	RCV000226629.1,