rs1060499813

Orientation

minus

Stabilized

minus

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

Make rs1060499813(-;-)

Make rs1060499813(-;TCAA)

Reference

GRCh38.p7 38.3/150

Chromosome

16

Position

23635496

Gene

PALB2

is a	snp
is	mentioned by
dbSNP	rs1060499813
dbSNP (classic)	rs1060499813
ClinGen	rs1060499813
ebi	rs1060499813
HLI	rs1060499813
Exac	rs1060499813
Gnomad	rs1060499813
Varsome	rs1060499813
LitVar	rs1060499813
Map	rs1060499813
PheGenI	rs1060499813
Biobank	rs1060499813
1000 genomes	rs1060499813
hgdp	rs1060499813
ensembl	rs1060499813
geneview	rs1060499813
scholar	rs1060499813
google	rs1060499813
pharmgkb	rs1060499813
gwascentral	rs1060499813
openSNP	rs1060499813
23andMe	rs1060499813
SNPshot	rs1060499813
SNPdbe	rs1060499813
MSV3d	rs1060499813
GWAS Ctlg	rs1060499813

Max Magnitude

0

ClinVar
Risk	rs1060499813(-;-)
Alt	rs1060499813(-;-)
Reference	Rs1060499813(TCAA;TCAA)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	PALB2
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000016.9:g.23646817_23646820delTTGA
CLNSRC
CLNACC	RCV000454229.1,