rs1060499821

Orientation

minus

Stabilized

minus

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

Make rs1060499821(C;C)

Make rs1060499821(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

16

Position

23626234

Gene

PALB2

is a	snp
is	mentioned by
dbSNP	rs1060499821
dbSNP (classic)	rs1060499821
ClinGen	rs1060499821
ebi	rs1060499821
HLI	rs1060499821
Exac	rs1060499821
Gnomad	rs1060499821
Varsome	rs1060499821
LitVar	rs1060499821
Map	rs1060499821
PheGenI	rs1060499821
Biobank	rs1060499821
1000 genomes	rs1060499821
hgdp	rs1060499821
ensembl	rs1060499821
geneview	rs1060499821
scholar	rs1060499821
google	rs1060499821
pharmgkb	rs1060499821
gwascentral	rs1060499821
openSNP	rs1060499821
23andMe	rs1060499821
SNPshot	rs1060499821
SNPdbe	rs1060499821
MSV3d	rs1060499821
GWAS Ctlg	rs1060499821

Max Magnitude

0

ClinVar
Risk	rs1060499821(C;C)
Alt	rs1060499821(C;C)
Reference	Rs1060499821(T;T)
Significance	Probable-Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	PALB2
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000016.9:g.23637555A>G
CLNSRC
CLNACC	RCV000454214.1,