rs587776424

Orientation

minus

Stabilized

minus

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

Make rs587776424(CTTA;CTTA)

Reference

GRCh38 38.1/142

Chromosome

16

Position

23603594

Gene

PALB2

is a	snp
is	mentioned by
dbSNP	rs587776424
dbSNP (classic)	rs587776424
ClinGen	rs587776424
ebi	rs587776424
HLI	rs587776424
Exac	rs587776424
Gnomad	rs587776424
Varsome	rs587776424
LitVar	rs587776424
Map	rs587776424
PheGenI	rs587776424
Biobank	rs587776424
1000 genomes	rs587776424
hgdp	rs587776424
ensembl	rs587776424
geneview	rs587776424
scholar	rs587776424
google	rs587776424
pharmgkb	rs587776424
gwascentral	rs587776424
openSNP	rs587776424
23andMe	rs587776424
SNPshot	rs587776424
SNPdbe	rs587776424
MSV3d	rs587776424
GWAS Ctlg	rs587776424

Merged from

Rs751415161

Max Magnitude

7

ClinVar
Risk	Rs587776424(ACTT;ACTT) Rs587776424(-;-)
Alt	Rs587776424(ACTT;ACTT) Rs587776424(-;-)
Reference	rs587776424(CTTA;CTTA)
Significance	Other
Disease	not provided Hereditary cancer-predisposing syndrome
Variation	info
Gene	PALB2
CLNDBN	not provided Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000016.9:g.23614912_23614915delAAGT
CLNSRC	ClinVar
CLNACC	RCV000133486.1, RCV000165289.3,