rs876658348

Orientation

minus

Stabilized

minus

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

Make rs876658348(-;-)

Make rs876658348(-;T)

Reference

GRCh38.p2 38.2/147

Chromosome

16

Position

23629684

Gene

PALB2

is a	snp
is	mentioned by
dbSNP	rs876658348
dbSNP (classic)	rs876658348
ClinGen	rs876658348
ebi	rs876658348
HLI	rs876658348
Exac	rs876658348
Gnomad	rs876658348
Varsome	rs876658348
LitVar	rs876658348
Map	rs876658348
PheGenI	rs876658348
Biobank	rs876658348
1000 genomes	rs876658348
hgdp	rs876658348
ensembl	rs876658348
geneview	rs876658348
scholar	rs876658348
google	rs876658348
pharmgkb	rs876658348
gwascentral	rs876658348
openSNP	rs876658348
23andMe	rs876658348
SNPshot	rs876658348
SNPdbe	rs876658348
MSV3d	rs876658348
GWAS Ctlg	rs876658348

Max Magnitude

0

ClinVar
Risk	rs876658348(-;-)
Alt	rs876658348(-;-)
Reference	Rs876658348(T;T)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	PALB2
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000016.9:g.23641005delA
CLNSRC
CLNACC	RCV000217072.2,