rs1060499818

Orientation

minus

Stabilized

minus

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

Make rs1060499818(-;-)

Make rs1060499818(-;TT)

Reference

GRCh38.p7 38.3/150

Chromosome

16

Position

23630336

Gene

PALB2

is a	snp
is	mentioned by
dbSNP	rs1060499818
dbSNP (classic)	rs1060499818
ClinGen	rs1060499818
ebi	rs1060499818
HLI	rs1060499818
Exac	rs1060499818
Gnomad	rs1060499818
Varsome	rs1060499818
LitVar	rs1060499818
Map	rs1060499818
PheGenI	rs1060499818
Biobank	rs1060499818
1000 genomes	rs1060499818
hgdp	rs1060499818
ensembl	rs1060499818
geneview	rs1060499818
scholar	rs1060499818
google	rs1060499818
pharmgkb	rs1060499818
gwascentral	rs1060499818
openSNP	rs1060499818
23andMe	rs1060499818
SNPshot	rs1060499818
SNPdbe	rs1060499818
MSV3d	rs1060499818
GWAS Ctlg	rs1060499818

Max Magnitude

0

ClinVar
Risk	rs1060499818(-;-)
Alt	rs1060499818(-;-)
Reference	Rs1060499818(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.23641657_23641658delAA
CLNSRC
CLNACC	RCV000454322.1,