rs587776426

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(;)	0	common in clinvar
(-;-)	0	common/normal
(-;A)	5	PALB2-related cancer risk
(A;A)	7	Fanconi anemia, complementation group N

Reference

GRCh38 38.1/142

Chromosome

16

Position

23603563

Gene

PALB2

is a	snp
is	mentioned by
dbSNP	rs587776426
dbSNP (classic)	rs587776426
ClinGen	rs587776426
ebi	rs587776426
HLI	rs587776426
Exac	rs587776426
Gnomad	rs587776426
Varsome	rs587776426
LitVar	rs587776426
Map	rs587776426
PheGenI	rs587776426
Biobank	rs587776426
1000 genomes	rs587776426
hgdp	rs587776426
ensembl	rs587776426
geneview	rs587776426
scholar	rs587776426
google	rs587776426
pharmgkb	rs587776426
gwascentral	rs587776426
openSNP	rs587776426
23andMe	rs587776426
SNPshot	rs587776426
SNPdbe	rs587776426
MSV3d	rs587776426
GWAS Ctlg	rs587776426

Max Magnitude

7

ClinVar
Risk	Rs587776426(A;A)
Alt	Rs587776426(A;A)
Reference	Rs587776426(-;-)
Significance	Pathogenic
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.23614885dupT
CLNSRC	ClinVar GeneDx
CLNACC	RCV000116106.4, RCV000133488.2, RCV000200796.3,