rs730881867

Orientation

minus

Stabilized

minus

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

Reference

GRCh38.p2 38.2/144

Chromosome

16

Position

23630000

Gene

PALB2

is a	snp
is	mentioned by
dbSNP	rs730881867
dbSNP (classic)	rs730881867
ClinGen	rs730881867
ebi	rs730881867
HLI	rs730881867
Exac	rs730881867
Gnomad	rs730881867
Varsome	rs730881867
LitVar	rs730881867
Map	rs730881867
PheGenI	rs730881867
Biobank	rs730881867
1000 genomes	rs730881867
hgdp	rs730881867
ensembl	rs730881867
geneview	rs730881867
scholar	rs730881867
google	rs730881867
pharmgkb	rs730881867
gwascentral	rs730881867
openSNP	rs730881867
23andMe	rs730881867
SNPshot	rs730881867
SNPdbe	rs730881867
MSV3d	rs730881867
GWAS Ctlg	rs730881867

Max Magnitude

7

ClinVar
Risk	Rs730881867(-;-)
Alt	Rs730881867(-;-)
Reference	Rs730881867(G;G)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	PALB2
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000016.9:g.23641321delC
CLNSRC
CLNACC	RCV000160808.1,