rs730881871

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(-;-)	7	Fanconi anemia, complementation group N
(-;C)	5	PALB2-related cancer risk
(C;C)	0	common in clinvar

Reference

GRCh38.p2 38.2/144

Chromosome

16

Position

23635598

Gene

PALB2

is a	snp
is	mentioned by
dbSNP	rs730881871
dbSNP (classic)	rs730881871
ClinGen	rs730881871
ebi	rs730881871
HLI	rs730881871
Exac	rs730881871
Gnomad	rs730881871
Varsome	rs730881871
LitVar	rs730881871
Map	rs730881871
PheGenI	rs730881871
Biobank	rs730881871
1000 genomes	rs730881871
hgdp	rs730881871
ensembl	rs730881871
geneview	rs730881871
scholar	rs730881871
google	rs730881871
pharmgkb	rs730881871
gwascentral	rs730881871
openSNP	rs730881871
23andMe	rs730881871
SNPshot	rs730881871
SNPdbe	rs730881871
MSV3d	rs730881871
GWAS Ctlg	rs730881871

Max Magnitude

7

ClinVar
Risk	Rs730881871(-;-)
Alt	Rs730881871(-;-)
Reference	Rs730881871(C;C)
Significance	Pathogenic
Disease	not provided Hereditary cancer-predisposing syndrome Familial cancer of breast
Variation	info
Gene	PALB2
CLNDBN	not provided Hereditary cancer-predisposing syndrome Familial cancer of breast
Reversed	1
HGVS	NC_000016.9:g.23646919delG
CLNSRC
CLNACC	RCV000160813.2, RCV000454254.1, RCV000463598.1,