rs1060499831

Orientation

minus

Stabilized

minus

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

Make rs1060499831(A;T)

Make rs1060499831(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

16

Position

23635615

Gene

PALB2

is a	snp
is	mentioned by
dbSNP	rs1060499831
dbSNP (classic)	rs1060499831
ClinGen	rs1060499831
ebi	rs1060499831
HLI	rs1060499831
Exac	rs1060499831
Gnomad	rs1060499831
Varsome	rs1060499831
LitVar	rs1060499831
Map	rs1060499831
PheGenI	rs1060499831
Biobank	rs1060499831
1000 genomes	rs1060499831
hgdp	rs1060499831
ensembl	rs1060499831
geneview	rs1060499831
scholar	rs1060499831
google	rs1060499831
pharmgkb	rs1060499831
gwascentral	rs1060499831
openSNP	rs1060499831
23andMe	rs1060499831
SNPshot	rs1060499831
SNPdbe	rs1060499831
MSV3d	rs1060499831
GWAS Ctlg	rs1060499831

Max Magnitude

0

ClinVar
Risk	rs1060499831(T;T)
Alt	rs1060499831(T;T)
Reference	Rs1060499831(A;A)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	PALB2
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000016.9:g.23646936T>A
CLNSRC
CLNACC	RCV000454180.1,