rs876658358

Orientation

minus

Stabilized

minus

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

Make rs876658358(AAGGTACAAT;AAGGTACAAT)

Make rs876658358(AAGGTACAAT;TGCCAGGAGCTGCATAAACATTC)

Reference

GRCh38.p2 38.2/147

Chromosome

16

Position

23629650

Gene

PALB2

is a	snp
is	mentioned by
dbSNP	rs876658358
dbSNP (classic)	rs876658358
ClinGen	rs876658358
ebi	rs876658358
HLI	rs876658358
Exac	rs876658358
Gnomad	rs876658358
Varsome	rs876658358
LitVar	rs876658358
Map	rs876658358
PheGenI	rs876658358
Biobank	rs876658358
1000 genomes	rs876658358
hgdp	rs876658358
ensembl	rs876658358
geneview	rs876658358
scholar	rs876658358
google	rs876658358
pharmgkb	rs876658358
gwascentral	rs876658358
openSNP	rs876658358
23andMe	rs876658358
SNPshot	rs876658358
SNPdbe	rs876658358
MSV3d	rs876658358
GWAS Ctlg	rs876658358

Max Magnitude

0

ClinVar
Risk	rs876658358(AAGGTACAAT;AAGGTACAAT)
Alt	rs876658358(AAGGTACAAT;AAGGTACAAT)
Reference	Rs876658358(TGCCAGGAGCTGCATAAACATTC;TGCCAGGAGCTGCATAAACATTC)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	PALB2
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000016.9:g.23640971_23640993del23insATTGTACCTT
CLNSRC
CLNACC	RCV000216440.1,