rs1060499819

Orientation

minus

Stabilized

minus

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

Make rs1060499819(-;-)

Make rs1060499819(-;C)

Reference

GRCh38.p7 38.3/150

Chromosome

16

Position

23630062

Gene

PALB2

is a	snp
is	mentioned by
dbSNP	rs1060499819
dbSNP (classic)	rs1060499819
ClinGen	rs1060499819
ebi	rs1060499819
HLI	rs1060499819
Exac	rs1060499819
Gnomad	rs1060499819
Varsome	rs1060499819
LitVar	rs1060499819
Map	rs1060499819
PheGenI	rs1060499819
Biobank	rs1060499819
1000 genomes	rs1060499819
hgdp	rs1060499819
ensembl	rs1060499819
geneview	rs1060499819
scholar	rs1060499819
google	rs1060499819
pharmgkb	rs1060499819
gwascentral	rs1060499819
openSNP	rs1060499819
23andMe	rs1060499819
SNPshot	rs1060499819
SNPdbe	rs1060499819
MSV3d	rs1060499819
GWAS Ctlg	rs1060499819

Max Magnitude

0

ClinVar
Risk	rs1060499819(-;-)
Alt	rs1060499819(-;-)
Reference	Rs1060499819(C;C)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	PALB2
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000016.9:g.23641383delG
CLNSRC
CLNACC	RCV000454277.1,