rs587781411

Merged into

rs587776428

Orientation

minus

Stabilized

minus

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

Reference

GRCh38.p2 38.2/144

Chromosome

16

Position

23603512

Gene

PALB2

is a	snp
is	mentioned by
dbSNP	rs587781411
dbSNP (classic)	rs587781411
ClinGen	rs587781411
ebi	rs587781411
HLI	rs587781411
Exac	rs587781411
Gnomad	rs587781411
Varsome	rs587781411
LitVar	rs587781411
Map	rs587781411
PheGenI	rs587781411
Biobank	rs587781411
1000 genomes	rs587781411
hgdp	rs587781411
ensembl	rs587781411
geneview	rs587781411
scholar	rs587781411
google	rs587781411
pharmgkb	rs587781411
gwascentral	rs587781411
openSNP	rs587781411
23andMe	rs587781411
SNPshot	rs587781411
SNPdbe	rs587781411
MSV3d	rs587781411
GWAS Ctlg	rs587781411

Status

Merged into rs587776428

Max Magnitude

7

ClinVar
Risk
Alt
Reference	Rs587781411(TC;TC)
Significance	Other
Disease	Hereditary cancer-predisposing syndrome not provided Familial cancer of breast
Variation	info
Gene	PALB2
CLNDBN	Hereditary cancer-predisposing syndrome not provided Familial cancer of breast
Reversed	1
HGVS	NC_000016.9:g.23614833_23614834delGA
CLNSRC
CLNACC	RCV000129272.3, RCV000133490.2, RCV000211073.2,