rs786203382

Orientation

minus

Stabilized

minus

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

Reference

GRCh38.p2 38.2/146

Chromosome

16

Position

23629255

Gene

PALB2

is a	snp
is	mentioned by
dbSNP	rs786203382
dbSNP (classic)	rs786203382
ClinGen	rs786203382
ebi	rs786203382
HLI	rs786203382
Exac	rs786203382
Gnomad	rs786203382
Varsome	rs786203382
LitVar	rs786203382
Map	rs786203382
PheGenI	rs786203382
Biobank	rs786203382
1000 genomes	rs786203382
hgdp	rs786203382
ensembl	rs786203382
geneview	rs786203382
scholar	rs786203382
google	rs786203382
pharmgkb	rs786203382
gwascentral	rs786203382
openSNP	rs786203382
23andMe	rs786203382
SNPshot	rs786203382
SNPdbe	rs786203382
MSV3d	rs786203382
GWAS Ctlg	rs786203382

Max Magnitude

7

ClinVar
Risk	Rs786203382(TCAGA;TCAGA)
Alt	Rs786203382(TCAGA;TCAGA)
Reference	Rs786203382(GCAGAGCTTCCT;GCAGAGCTTCCT)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	PALB2
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000016.9:g.23640576_23640587delAGGAAGCTCTGCinsTCTGA
CLNSRC
CLNACC	RCV000166663.1,