rs587776411

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common in clinvar
(C;T)	3	significantly increased risk of breast cancer
(T;T)	7	Fanconi anemia, complementation group N

Reference

GRCh38 38.1/142

Chromosome

16

Position

23635438

Gene

PALB2

is a	snp
is	mentioned by
dbSNP	rs587776411
dbSNP (classic)	rs587776411
ClinGen	rs587776411
ebi	rs587776411
HLI	rs587776411
Exac	rs587776411
Gnomad	rs587776411
Varsome	rs587776411
LitVar	rs587776411
Map	rs587776411
PheGenI	rs587776411
Biobank	rs587776411
1000 genomes	rs587776411
hgdp	rs587776411
ensembl	rs587776411
geneview	rs587776411
scholar	rs587776411
google	rs587776411
pharmgkb	rs587776411
gwascentral	rs587776411
openSNP	rs587776411
23andMe	rs587776411
SNPshot	rs587776411
SNPdbe	rs587776411
MSV3d	rs587776411
GWAS Ctlg	rs587776411

Max Magnitude

7

ClinVar
Risk	Rs587776411(T;T)
Alt	Rs587776411(T;T)
Reference	Rs587776411(C;C)
Significance	Other
Disease	not provided
Variation	info
Gene	PALB2
CLNDBN	not provided
Reversed	1
HGVS	NC_000016.9:g.23646759G>A
CLNSRC	ClinVar
CLNACC	RCV000133472.1,