rs786203346

Orientation

minus

Stabilized

minus

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

Reference

GRCh38.p2 38.2/146

Chromosome

16

Position

23634928

Gene

PALB2

is a	snp
is	mentioned by
dbSNP	rs786203346
dbSNP (classic)	rs786203346
ClinGen	rs786203346
ebi	rs786203346
HLI	rs786203346
Exac	rs786203346
Gnomad	rs786203346
Varsome	rs786203346
LitVar	rs786203346
Map	rs786203346
PheGenI	rs786203346
Biobank	rs786203346
1000 genomes	rs786203346
hgdp	rs786203346
ensembl	rs786203346
geneview	rs786203346
scholar	rs786203346
google	rs786203346
pharmgkb	rs786203346
gwascentral	rs786203346
openSNP	rs786203346
23andMe	rs786203346
SNPshot	rs786203346
SNPdbe	rs786203346
MSV3d	rs786203346
GWAS Ctlg	rs786203346

Max Magnitude

7

ClinVar
Risk	Rs786203346(TT;TT)
Alt	Rs786203346(TT;TT)
Reference	Rs786203346(-;-)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	PALB2
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000016.9:g.23646250_23646251dupAA
CLNSRC
CLNACC	RCV000166617.2,