rs587776428

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(-;-)	7	Fanconi anemia, complementation group N
(-;CT)	3	significantly increased risk of breast cancer
(TC;TC)	0	common in clinvar

Make rs587776428(CT;CT)

Reference

GRCh38 38.1/142

Chromosome

16

Position

23603515

Gene

PALB2

is a	snp
is	mentioned by
dbSNP	rs587776428
dbSNP (classic)	rs587776428
ClinGen	rs587776428
ebi	rs587776428
HLI	rs587776428
Exac	rs587776428
Gnomad	rs587776428
Varsome	rs587776428
LitVar	rs587776428
Map	rs587776428
PheGenI	rs587776428
Biobank	rs587776428
1000 genomes	rs587776428
hgdp	rs587776428
ensembl	rs587776428
geneview	rs587776428
scholar	rs587776428
google	rs587776428
pharmgkb	rs587776428
gwascentral	rs587776428
openSNP	rs587776428
23andMe	rs587776428
SNPshot	rs587776428
SNPdbe	rs587776428
MSV3d	rs587776428
GWAS Ctlg	rs587776428

Merged from

Rs587781411

Max Magnitude

7

ClinVar
Risk	Rs587776428(TC;TC) Rs587776428(-;-)
Alt	Rs587776428(TC;TC) Rs587776428(-;-)
Reference	rs587776428(CT;CT)
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	ClinVar
CLNACC	RCV000129272.4, RCV000133490.2, RCV000211073.2,