rs587780206

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(CA;CA)	0	common in clinvar
(CA;TG)	3	2-4 fold higher risk for breast cancer, depending on family history
(TG;TG)	7	Fanconi anemia, complementation group N

Reference

GRCh38.p2 38.2/144

Chromosome

16

Position

23634870

Gene

PALB2

is a	snp
is	mentioned by
dbSNP	rs587780206
dbSNP (classic)	rs587780206
ClinGen	rs587780206
ebi	rs587780206
HLI	rs587780206
Exac	rs587780206
Gnomad	rs587780206
Varsome	rs587780206
LitVar	rs587780206
Map	rs587780206
PheGenI	rs587780206
Biobank	rs587780206
1000 genomes	rs587780206
hgdp	rs587780206
ensembl	rs587780206
geneview	rs587780206
scholar	rs587780206
google	rs587780206
pharmgkb	rs587780206
gwascentral	rs587780206
openSNP	rs587780206
23andMe	rs587780206
SNPshot	rs587780206
SNPdbe	rs587780206
MSV3d	rs587780206
GWAS Ctlg	rs587780206

Max Magnitude

7

ClinVar
Risk	Rs587780206(TG;TG)
Alt	Rs587780206(TG;TG)
Reference	Rs587780206(CA;CA)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	PALB2
CLNDBN	Hereditary cancer-predisposing syndrome not provided
Reversed	1
HGVS	NC_000016.9:g.23646191_23646192delTGinsCA
CLNSRC
CLNACC	RCV000116070.5, RCV000235193.2,