rs587776417

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(G;G)	0	common/normal
(G;T)	3	significantly increased risk of breast cancer
(T;T)	7	Fanconi anemia, complementation group N

Reference

GRCh38 38.1/142

Chromosome

16

Position

23629276

Gene

PALB2

is a	snp
is	mentioned by
dbSNP	rs587776417
dbSNP (classic)	rs587776417
ClinGen	rs587776417
ebi	rs587776417
HLI	rs587776417
Exac	rs587776417
Gnomad	rs587776417
Varsome	rs587776417
LitVar	rs587776417
Map	rs587776417
PheGenI	rs587776417
Biobank	rs587776417
1000 genomes	rs587776417
hgdp	rs587776417
ensembl	rs587776417
geneview	rs587776417
scholar	rs587776417
google	rs587776417
pharmgkb	rs587776417
gwascentral	rs587776417
openSNP	rs587776417
23andMe	rs587776417
SNPshot	rs587776417
SNPdbe	rs587776417
MSV3d	rs587776417
GWAS Ctlg	rs587776417

Max Magnitude

7

ClinVar
Risk	rs587776417(C;C) Rs587776417(T;T)
Alt	rs587776417(C;C) Rs587776417(T;T)
Reference	Rs587776417(G;G)
Significance	Other
Disease	Pancreatic cancer 3 Familial cancer of breast not provided
Variation	info
Gene	PALB2
CLNDBN	Pancreatic cancer 3 Familial cancer of breast not provided
Reversed	1
HGVS	NC_000016.9:g.23640597C>A; NC_000016.9:g.23640597C>G
CLNSRC	OMIM Allelic Variant PALB2 database
CLNACC	RCV000001312.2, RCV000114532.1, RCV000133479.1, RCV000198016.1,