rs1060499814

Orientation

minus

Stabilized

minus

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

Make rs1060499814(A;A)

Make rs1060499814(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

16

Position

23638069

Gene

PALB2

is a	snp
is	mentioned by
dbSNP	rs1060499814
dbSNP (classic)	rs1060499814
ClinGen	rs1060499814
ebi	rs1060499814
HLI	rs1060499814
Exac	rs1060499814
Gnomad	rs1060499814
Varsome	rs1060499814
LitVar	rs1060499814
Map	rs1060499814
PheGenI	rs1060499814
Biobank	rs1060499814
1000 genomes	rs1060499814
hgdp	rs1060499814
ensembl	rs1060499814
geneview	rs1060499814
scholar	rs1060499814
google	rs1060499814
pharmgkb	rs1060499814
gwascentral	rs1060499814
openSNP	rs1060499814
23andMe	rs1060499814
SNPshot	rs1060499814
SNPdbe	rs1060499814
MSV3d	rs1060499814
GWAS Ctlg	rs1060499814

Max Magnitude

0

ClinVar
Risk	rs1060499814(A;A)
Alt	rs1060499814(A;A)
Reference	Rs1060499814(G;G)
Significance	Probable-Pathogenic
Disease	Hereditary cancer-predisposing syndrome Familial cancer of breast not provided
Variation	info
Gene	PALB2
CLNDBN	Hereditary cancer-predisposing syndrome Familial cancer of breast not provided
Reversed	1
HGVS	NC_000016.9:g.23649390C>T
CLNSRC
CLNACC	RCV000454354.1, RCV000466548.1, RCV000484652.1,