rs864622636

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common in clinvar
(C;T)	7	Pancreatic cancer/Melanoma Syndrome

Make rs864622636(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

9

Position

21974680

Gene

CDKN2A

is a	snp
is	mentioned by
dbSNP	rs864622636
dbSNP (classic)	rs864622636
ClinGen	rs864622636
ebi	rs864622636
HLI	rs864622636
Exac	rs864622636
Gnomad	rs864622636
Varsome	rs864622636
LitVar	rs864622636
Map	rs864622636
PheGenI	rs864622636
Biobank	rs864622636
1000 genomes	rs864622636
hgdp	rs864622636
ensembl	rs864622636
geneview	rs864622636
scholar	rs864622636
google	rs864622636
pharmgkb	rs864622636
gwascentral	rs864622636
openSNP	rs864622636
23andMe	rs864622636
SNPshot	rs864622636
SNPdbe	rs864622636
MSV3d	rs864622636
GWAS Ctlg	rs864622636

Max Magnitude

7

ClinVar
Risk	rs864622636(T;T)
Alt	rs864622636(T;T)
Reference	Rs864622636(C;C)
Significance	Pathogenic
Disease	Hereditary cutaneous melanoma Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	CDKN2A
CLNDBN	Hereditary cutaneous melanoma Hereditary cancer-predisposing syndrome not provided
Reversed	1
HGVS	NC_000009.11:g.21974679G>A
CLNSRC
CLNACC	RCV000206296.3, RCV000221580.2, RCV000485187.1,