rs730881879

Orientation

minus

Stabilized

minus

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

Reference

GRCh38.p2 38.2/144

Chromosome

16

Position

23636336

Gene

PALB2

is a	snp
is	mentioned by
dbSNP	rs730881879
dbSNP (classic)	rs730881879
ClinGen	rs730881879
ebi	rs730881879
HLI	rs730881879
Exac	rs730881879
Gnomad	rs730881879
Varsome	rs730881879
LitVar	rs730881879
Map	rs730881879
PheGenI	rs730881879
Biobank	rs730881879
1000 genomes	rs730881879
hgdp	rs730881879
ensembl	rs730881879
geneview	rs730881879
scholar	rs730881879
google	rs730881879
pharmgkb	rs730881879
gwascentral	rs730881879
openSNP	rs730881879
23andMe	rs730881879
SNPshot	rs730881879
SNPdbe	rs730881879
MSV3d	rs730881879
GWAS Ctlg	rs730881879

Max Magnitude

7

ClinVar
Risk	Rs730881879(G;G)
Alt	Rs730881879(G;G)
Reference	Rs730881879(A;A)
Significance	Probable-Pathogenic
Disease	not provided Familial cancer of breast Hereditary cancer-predisposing syndrome
Variation	info
Gene	PALB2
CLNDBN	not provided Familial cancer of breast Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000016.9:g.23647657T>C
CLNSRC
CLNACC	RCV000160830.3, RCV000206312.3, RCV000213220.1,