rs587776527

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	7	Fanconi anemia, complementation group N
(A;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

23607958

Gene

PALB2

is a	snp
is	mentioned by
dbSNP	rs587776527
dbSNP (classic)	rs587776527
ClinGen	rs587776527
ebi	rs587776527
HLI	rs587776527
Exac	rs587776527
Gnomad	rs587776527
Varsome	rs587776527
LitVar	rs587776527
Map	rs587776527
PheGenI	rs587776527
Biobank	rs587776527
1000 genomes	rs587776527
hgdp	rs587776527
ensembl	rs587776527
geneview	rs587776527
scholar	rs587776527
google	rs587776527
pharmgkb	rs587776527
gwascentral	rs587776527
openSNP	rs587776527
23andMe	rs587776527
SNPshot	rs587776527
SNPdbe	rs587776527
MSV3d	rs587776527
GWAS Ctlg	rs587776527

Max Magnitude

7

ClinVar
Risk	Rs587776527(A;A) rs587776527(C;C)
Alt	Rs587776527(A;A) rs587776527(C;C)
Reference	Rs587776527(G;G)
Significance	Other
Disease	Pancreatic cancer 3 Hereditary cancer-predisposing syndrome Familial cancer of breast not provided
Variation	info
Gene	PALB2
CLNDBN	Pancreatic cancer 3 Hereditary cancer-predisposing syndrome Familial cancer of breast not provided
Reversed	0
HGVS	NC_000016.9:g.23619279G>A; NC_000016.9:g.23619279G>C
CLNSRC	OMIM Allelic Variant PALB2 database
CLNACC	RCV000114612.3, RCV000160853.4, RCV000168017.3, RCV000212825.2, RCV000461441.1,