rs730881888

Orientation

minus

Stabilized

minus

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

Reference

GRCh38.p2 38.2/144

Chromosome

16

Position

23629925

Gene

PALB2

is a	snp
is	mentioned by
dbSNP	rs730881888
dbSNP (classic)	rs730881888
ClinGen	rs730881888
ebi	rs730881888
HLI	rs730881888
Exac	rs730881888
Gnomad	rs730881888
Varsome	rs730881888
LitVar	rs730881888
Map	rs730881888
PheGenI	rs730881888
Biobank	rs730881888
1000 genomes	rs730881888
hgdp	rs730881888
ensembl	rs730881888
geneview	rs730881888
scholar	rs730881888
google	rs730881888
pharmgkb	rs730881888
gwascentral	rs730881888
openSNP	rs730881888
23andMe	rs730881888
SNPshot	rs730881888
SNPdbe	rs730881888
MSV3d	rs730881888
GWAS Ctlg	rs730881888

Max Magnitude

7

ClinVar
Risk	Rs730881888(A;A) rs730881888(C;C)
Alt	Rs730881888(A;A) rs730881888(C;C)
Reference	Rs730881888(T;T)
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.23641246A>G; NC_000016.9:g.23641246A>T
CLNSRC
CLNACC	RCV000199909.1, RCV000219447.1, RCV000160839.2,