rs1060499828

Orientation

minus

Stabilized

minus

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

Make rs1060499828(-;-)

Make rs1060499828(-;G)

Reference

GRCh38.p7 38.3/150

Chromosome

16

Position

23607903

Gene

PALB2

is a	snp
is	mentioned by
dbSNP	rs1060499828
dbSNP (classic)	rs1060499828
ClinGen	rs1060499828
ebi	rs1060499828
HLI	rs1060499828
Exac	rs1060499828
Gnomad	rs1060499828
Varsome	rs1060499828
LitVar	rs1060499828
Map	rs1060499828
PheGenI	rs1060499828
Biobank	rs1060499828
1000 genomes	rs1060499828
hgdp	rs1060499828
ensembl	rs1060499828
geneview	rs1060499828
scholar	rs1060499828
google	rs1060499828
pharmgkb	rs1060499828
gwascentral	rs1060499828
openSNP	rs1060499828
23andMe	rs1060499828
SNPshot	rs1060499828
SNPdbe	rs1060499828
MSV3d	rs1060499828
GWAS Ctlg	rs1060499828

Max Magnitude

0

ClinVar
Risk	rs1060499828(-;-)
Alt	rs1060499828(-;-)
Reference	Rs1060499828(G;G)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	PALB2
CLNDBN	Hereditary cancer-predisposing syndrome not provided
Reversed	1
HGVS	NC_000016.9:g.23619224delC
CLNSRC
CLNACC	RCV000454312.1, RCV000484224.1,