rs730881897

Orientation

minus

Stabilized

minus

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

Reference

GRCh38.p2 38.2/144

Chromosome

16

Position

23637954

Gene

PALB2

is a	snp
is	mentioned by
dbSNP	rs730881897
dbSNP (classic)	rs730881897
ClinGen	rs730881897
ebi	rs730881897
HLI	rs730881897
Exac	rs730881897
Gnomad	rs730881897
Varsome	rs730881897
LitVar	rs730881897
Map	rs730881897
PheGenI	rs730881897
Biobank	rs730881897
1000 genomes	rs730881897
hgdp	rs730881897
ensembl	rs730881897
geneview	rs730881897
scholar	rs730881897
google	rs730881897
pharmgkb	rs730881897
gwascentral	rs730881897
openSNP	rs730881897
23andMe	rs730881897
SNPshot	rs730881897
SNPdbe	rs730881897
MSV3d	rs730881897
GWAS Ctlg	rs730881897

Max Magnitude

7

ClinVar
Risk	Rs730881897(G;G)
Alt	Rs730881897(G;G)
Reference	Rs730881897(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	PALB2
CLNDBN	not provided
Reversed	1
HGVS	NC_000016.9:g.23649275T>C
CLNSRC
CLNACC	RCV000160858.2,