rs1060499829

Orientation

minus

Stabilized

minus

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

Make rs1060499829(-;-)

Make rs1060499829(-;G)

Reference

GRCh38.p7 38.3/150

Chromosome

16

Position

23641109

Gene	DCTN5, PALB2

is a	snp
is	mentioned by
dbSNP	rs1060499829
dbSNP (classic)	rs1060499829
ClinGen	rs1060499829
ebi	rs1060499829
HLI	rs1060499829
Exac	rs1060499829
Gnomad	rs1060499829
Varsome	rs1060499829
LitVar	rs1060499829
Map	rs1060499829
PheGenI	rs1060499829
Biobank	rs1060499829
1000 genomes	rs1060499829
hgdp	rs1060499829
ensembl	rs1060499829
geneview	rs1060499829
scholar	rs1060499829
google	rs1060499829
pharmgkb	rs1060499829
gwascentral	rs1060499829
openSNP	rs1060499829
23andMe	rs1060499829
SNPshot	rs1060499829
SNPdbe	rs1060499829
MSV3d	rs1060499829
GWAS Ctlg	rs1060499829

Max Magnitude

0

ClinVar
Risk	rs1060499829(-;-)
Alt	rs1060499829(-;-)
Reference	Rs1060499829(G;G)
Significance	Probable-Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	PALB2 DCTN5
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000016.9:g.23652430delC
CLNSRC
CLNACC	RCV000454282.1,