rs1060499817

Orientation

minus

Stabilized

minus

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

Make rs1060499817(-;-)

Make rs1060499817(-;TT)

Reference

GRCh38.p7 38.3/150

Chromosome

16

Position

23634954

Gene

PALB2

is a	snp
is	mentioned by
dbSNP	rs1060499817
dbSNP (classic)	rs1060499817
ClinGen	rs1060499817
ebi	rs1060499817
HLI	rs1060499817
Exac	rs1060499817
Gnomad	rs1060499817
Varsome	rs1060499817
LitVar	rs1060499817
Map	rs1060499817
PheGenI	rs1060499817
Biobank	rs1060499817
1000 genomes	rs1060499817
hgdp	rs1060499817
ensembl	rs1060499817
geneview	rs1060499817
scholar	rs1060499817
google	rs1060499817
pharmgkb	rs1060499817
gwascentral	rs1060499817
openSNP	rs1060499817
23andMe	rs1060499817
SNPshot	rs1060499817
SNPdbe	rs1060499817
MSV3d	rs1060499817
GWAS Ctlg	rs1060499817

Max Magnitude

0

ClinVar
Risk	rs1060499817(-;-)
Alt	rs1060499817(-;-)
Reference	Rs1060499817(TT;TT)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	PALB2
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000016.9:g.23646275_23646276delAA
CLNSRC
CLNACC	RCV000454252.1,