rs786203892

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(-;-)	7	Fanconi anemia, complementation group N
(-;AGGTAA)	3	2-4 fold higher risk for breast cancer, depending on family history
(AGGTAA;AGGTAA)	0	common in clinvar

Reference

GRCh38.p2 38.2/146

Chromosome

16

Position

23626232

Gene

PALB2

is a	snp
is	mentioned by
dbSNP	rs786203892
dbSNP (classic)	rs786203892
ClinGen	rs786203892
ebi	rs786203892
HLI	rs786203892
Exac	rs786203892
Gnomad	rs786203892
Varsome	rs786203892
LitVar	rs786203892
Map	rs786203892
PheGenI	rs786203892
Biobank	rs786203892
1000 genomes	rs786203892
hgdp	rs786203892
ensembl	rs786203892
geneview	rs786203892
scholar	rs786203892
google	rs786203892
pharmgkb	rs786203892
gwascentral	rs786203892
openSNP	rs786203892
23andMe	rs786203892
SNPshot	rs786203892
SNPdbe	rs786203892
MSV3d	rs786203892
GWAS Ctlg	rs786203892

Max Magnitude

7

ClinVar
Risk	Rs786203892(-;-)
Alt	Rs786203892(-;-)
Reference	Rs786203892(AGGTAA;AGGTAA)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	PALB2
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000016.9:g.23637553_23637558delTTACCT
CLNSRC
CLNACC	RCV000167394.1,