rs1060499812

Orientation

minus

Stabilized

minus

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

Make rs1060499812(G;T)

Make rs1060499812(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

16

Position

23635507

Gene

PALB2

is a	snp
is	mentioned by
dbSNP	rs1060499812
dbSNP (classic)	rs1060499812
ClinGen	rs1060499812
ebi	rs1060499812
HLI	rs1060499812
Exac	rs1060499812
Gnomad	rs1060499812
Varsome	rs1060499812
LitVar	rs1060499812
Map	rs1060499812
PheGenI	rs1060499812
Biobank	rs1060499812
1000 genomes	rs1060499812
hgdp	rs1060499812
ensembl	rs1060499812
geneview	rs1060499812
scholar	rs1060499812
google	rs1060499812
pharmgkb	rs1060499812
gwascentral	rs1060499812
openSNP	rs1060499812
23andMe	rs1060499812
SNPshot	rs1060499812
SNPdbe	rs1060499812
MSV3d	rs1060499812
GWAS Ctlg	rs1060499812

Max Magnitude

0

ClinVar
Risk	rs1060499812(T;T)
Alt	rs1060499812(T;T)
Reference	Rs1060499812(G;G)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	PALB2
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000016.9:g.23646828C>A
CLNSRC
CLNACC	RCV000454356.1,