rs1060499830

Orientation

minus

Stabilized

minus

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

Make rs1060499830(-;-)

Make rs1060499830(-;A)

Reference

GRCh38.p7 38.3/150

Chromosome

16

Position

23635787

Gene

PALB2

is a	snp
is	mentioned by
dbSNP	rs1060499830
dbSNP (classic)	rs1060499830
ClinGen	rs1060499830
ebi	rs1060499830
HLI	rs1060499830
Exac	rs1060499830
Gnomad	rs1060499830
Varsome	rs1060499830
LitVar	rs1060499830
Map	rs1060499830
PheGenI	rs1060499830
Biobank	rs1060499830
1000 genomes	rs1060499830
hgdp	rs1060499830
ensembl	rs1060499830
geneview	rs1060499830
scholar	rs1060499830
google	rs1060499830
pharmgkb	rs1060499830
gwascentral	rs1060499830
openSNP	rs1060499830
23andMe	rs1060499830
SNPshot	rs1060499830
SNPdbe	rs1060499830
MSV3d	rs1060499830
GWAS Ctlg	rs1060499830

Max Magnitude

0

ClinVar
Risk	rs1060499830(-;-)
Alt	rs1060499830(-;-)
Reference	Rs1060499830(A;A)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Familial cancer of breast
Variation	info
Gene	PALB2
CLNDBN	Hereditary cancer-predisposing syndrome Familial cancer of breast
Reversed	1
HGVS	NC_000016.9:g.23647108delT
CLNSRC
CLNACC	RCV000454341.1, RCV000458746.1,