rs587776416

Orientation

minus

Stabilized

minus

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

Reference

GRCh38 38.1/142

Chromosome

16

Position

23629986

Gene

PALB2

is a	snp
is	mentioned by
dbSNP	rs587776416
dbSNP (classic)	rs587776416
ClinGen	rs587776416
ebi	rs587776416
HLI	rs587776416
Exac	rs587776416
Gnomad	rs587776416
Varsome	rs587776416
LitVar	rs587776416
Map	rs587776416
PheGenI	rs587776416
Biobank	rs587776416
1000 genomes	rs587776416
hgdp	rs587776416
ensembl	rs587776416
geneview	rs587776416
scholar	rs587776416
google	rs587776416
pharmgkb	rs587776416
gwascentral	rs587776416
openSNP	rs587776416
23andMe	rs587776416
SNPshot	rs587776416
SNPdbe	rs587776416
MSV3d	rs587776416
GWAS Ctlg	rs587776416

Max Magnitude

7

ClinVar
Risk	Rs587776416(-;-)
Alt	Rs587776416(-;-)
Reference	Rs587776416(AT;AT)
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.23641307_23641308delAT
CLNSRC	Ambry Genetics ClinVar
CLNACC	RCV000123337.4, RCV000129400.5, RCV000133478.3,