rs587776410

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(-;-)	7	Fanconi anemia, complementation group N
(-;AAGAA)	5	PALB2-related cancer risk
(AAGAA;AAGAA)	0	common in clinvar

Reference

GRCh38 38.1/142

Chromosome

16

Position

23635505

Gene

PALB2

is a	snp
is	mentioned by
dbSNP	rs587776410
dbSNP (classic)	rs587776410
ClinGen	rs587776410
ebi	rs587776410
HLI	rs587776410
Exac	rs587776410
Gnomad	rs587776410
Varsome	rs587776410
LitVar	rs587776410
Map	rs587776410
PheGenI	rs587776410
Biobank	rs587776410
1000 genomes	rs587776410
hgdp	rs587776410
ensembl	rs587776410
geneview	rs587776410
scholar	rs587776410
google	rs587776410
pharmgkb	rs587776410
gwascentral	rs587776410
openSNP	rs587776410
23andMe	rs587776410
SNPshot	rs587776410
SNPdbe	rs587776410
MSV3d	rs587776410
GWAS Ctlg	rs587776410

Max Magnitude

7

ClinVar
Risk	Rs587776410(-;-)
Alt	Rs587776410(-;-)
Reference	Rs587776410(AAGAA;AAGAA)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome not provided Familial cancer of breast
Variation	info
Gene	PALB2
CLNDBN	Hereditary cancer-predisposing syndrome not provided Familial cancer of breast
Reversed	1
HGVS	NC_000016.9:g.23646826_23646830delTTCTT
CLNSRC	Ambry Genetics ClinVar
CLNACC	RCV000130093.3, RCV000133471.1, RCV000205410.2,