rs121913381

Orientation

minus

Stabilized

minus

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

Make rs121913381(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

9

Position

21971037

Gene

CDKN2A

is a	snp
is	mentioned by
dbSNP	rs121913381
dbSNP (classic)	rs121913381
ClinGen	rs121913381
ebi	rs121913381
HLI	rs121913381
Exac	rs121913381
Gnomad	rs121913381
Varsome	rs121913381
LitVar	rs121913381
Map	rs121913381
PheGenI	rs121913381
Biobank	rs121913381
1000 genomes	rs121913381
hgdp	rs121913381
ensembl	rs121913381
geneview	rs121913381
scholar	rs121913381
google	rs121913381
pharmgkb	rs121913381
gwascentral	rs121913381
openSNP	rs121913381
23andMe	rs121913381
SNPshot	rs121913381
SNPdbe	rs121913381
MSV3d	rs121913381
GWAS Ctlg	rs121913381

Max Magnitude

7

ClinVar
Risk	rs121913381(A;A) rs121913381(T;T)
Alt	rs121913381(A;A) rs121913381(T;T)
Reference	Rs121913381(G;G)
Significance	Probable-Pathogenic
Disease	Hereditary cancer-predisposing syndrome Neoplasm Hereditary cutaneous melanoma not specified
Variation	info
Gene	CDKN2A
CLNDBN	Hereditary cancer-predisposing syndrome Neoplasm Hereditary cutaneous melanoma not specified
Reversed	1
HGVS	NC_000009.11:g.21971036C>A; NC_000009.11:g.21971036C>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000160422.5, RCV000425594.1, RCV000198618.1, RCV000482818.1,