rs730881865

Orientation

minus

Stabilized

minus

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

Reference

GRCh38.p2 38.2/144

Chromosome

16

Position

23630230

Gene

PALB2

is a	snp
is	mentioned by
dbSNP	rs730881865
dbSNP (classic)	rs730881865
ClinGen	rs730881865
ebi	rs730881865
HLI	rs730881865
Exac	rs730881865
Gnomad	rs730881865
Varsome	rs730881865
LitVar	rs730881865
Map	rs730881865
PheGenI	rs730881865
Biobank	rs730881865
1000 genomes	rs730881865
hgdp	rs730881865
ensembl	rs730881865
geneview	rs730881865
scholar	rs730881865
google	rs730881865
pharmgkb	rs730881865
gwascentral	rs730881865
openSNP	rs730881865
23andMe	rs730881865
SNPshot	rs730881865
SNPdbe	rs730881865
MSV3d	rs730881865
GWAS Ctlg	rs730881865

Max Magnitude

7

ClinVar
Risk	Rs730881865(-;-)
Alt	Rs730881865(-;-)
Reference	Rs730881865(A;A)
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.23641551delT
CLNSRC
CLNACC	RCV000160805.4, RCV000212803.1, RCV000410708.1,