rs876660421

Orientation

plus

Stabilized

plus

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

Make rs876660421(-;-)

Make rs876660421(-;TT)

Reference

GRCh38.p2 38.2/147

Chromosome

13

Position

32340801

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs876660421
dbSNP (classic)	rs876660421
ClinGen	rs876660421
ebi	rs876660421
HLI	rs876660421
Exac	rs876660421
Gnomad	rs876660421
Varsome	rs876660421
LitVar	rs876660421
Map	rs876660421
PheGenI	rs876660421
Biobank	rs876660421
1000 genomes	rs876660421
hgdp	rs876660421
ensembl	rs876660421
geneview	rs876660421
scholar	rs876660421
google	rs876660421
pharmgkb	rs876660421
gwascentral	rs876660421
openSNP	rs876660421
23andMe	rs876660421
SNPshot	rs876660421
SNPdbe	rs876660421
MSV3d	rs876660421
GWAS Ctlg	rs876660421

Max Magnitude

0

ClinVar
Risk	rs876660421(-;-)
Alt	rs876660421(-;-)
Reference	Rs876660421(TT;TT)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	BRCA2
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000013.10:g.32914938_32914939delTT
CLNSRC
CLNACC	RCV000222779.1,