rs876659326

Orientation

minus

Stabilized

minus

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

Make rs876659326(-;-)

Make rs876659326(-;CCTTT)

Reference

GRCh38.p2 38.2/147

Chromosome

16

Position

23635797

Gene

PALB2

is a	snp
is	mentioned by
dbSNP	rs876659326
dbSNP (classic)	rs876659326
ClinGen	rs876659326
ebi	rs876659326
HLI	rs876659326
Exac	rs876659326
Gnomad	rs876659326
Varsome	rs876659326
LitVar	rs876659326
Map	rs876659326
PheGenI	rs876659326
Biobank	rs876659326
1000 genomes	rs876659326
hgdp	rs876659326
ensembl	rs876659326
geneview	rs876659326
scholar	rs876659326
google	rs876659326
pharmgkb	rs876659326
gwascentral	rs876659326
openSNP	rs876659326
23andMe	rs876659326
SNPshot	rs876659326
SNPdbe	rs876659326
MSV3d	rs876659326
GWAS Ctlg	rs876659326

Max Magnitude

0

ClinVar
Risk	rs876659326(-;-)
Alt	rs876659326(-;-)
Reference	Rs876659326(CCTTT;CCTTT)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	PALB2
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000016.9:g.23647118_23647122delAAAGG
CLNSRC
CLNACC	RCV000222919.1,