rs587776421

Merged into

rs180177126

Orientation

minus

Stabilized

minus

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

Reference

GRCh38 38.1/142

Chromosome

16

Position

23623045

Gene

PALB2

is a	snp
is	mentioned by
dbSNP	rs587776421
dbSNP (classic)	rs587776421
ClinGen	rs587776421
ebi	rs587776421
HLI	rs587776421
Exac	rs587776421
Gnomad	rs587776421
Varsome	rs587776421
LitVar	rs587776421
Map	rs587776421
PheGenI	rs587776421
Biobank	rs587776421
1000 genomes	rs587776421
hgdp	rs587776421
ensembl	rs587776421
geneview	rs587776421
scholar	rs587776421
google	rs587776421
pharmgkb	rs587776421
gwascentral	rs587776421
openSNP	rs587776421
23andMe	rs587776421
SNPshot	rs587776421
SNPdbe	rs587776421
MSV3d	rs587776421
GWAS Ctlg	rs587776421

Status

Merged into rs180177126

Max Magnitude

7

ClinVar
Risk
Alt
Reference	Rs587776421(AA;AA)
Significance	Pathogenic
Disease	Familial cancer of breast Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	PALB2
CLNDBN	Familial cancer of breast Hereditary cancer-predisposing syndrome not provided
Reversed	1
HGVS	NC_000016.9:g.23634365_23634366delTT
CLNSRC	PALB2 database
CLNACC	RCV000114575.3, RCV000132234.5, RCV000133483.2,