rs121913385

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs121913385(C;T)

Make rs121913385(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

9

Position

21971112

Gene

CDKN2A

is a	snp
is	mentioned by
dbSNP	rs121913385
dbSNP (classic)	rs121913385
ClinGen	rs121913385
ebi	rs121913385
HLI	rs121913385
Exac	rs121913385
Gnomad	rs121913385
Varsome	rs121913385
LitVar	rs121913385
Map	rs121913385
PheGenI	rs121913385
Biobank	rs121913385
1000 genomes	rs121913385
hgdp	rs121913385
ensembl	rs121913385
geneview	rs121913385
scholar	rs121913385
google	rs121913385
pharmgkb	rs121913385
gwascentral	rs121913385
openSNP	rs121913385
23andMe	rs121913385
SNPshot	rs121913385
SNPdbe	rs121913385
MSV3d	rs121913385
GWAS Ctlg	rs121913385

Max Magnitude

0

ClinVar
Risk	rs121913385(G;G) rs121913385(T;T)
Alt	rs121913385(G;G) rs121913385(T;T)
Reference	Rs121913385(C;C)
Significance	Probable-Pathogenic
Disease	Squamous cell carcinoma of the head and neck Adenocarcinoma of lung Transitional cell carcinoma of the bladder Neoplasm Pancreatic adenocarcinoma Adenocarcinoma of stomach Malignant melanoma of skin Squamous cell carcinoma of the skin Hepatocellular carcinoma
Variation	info
Gene	CDKN2A
CLNDBN	Squamous cell carcinoma of the head and neck Adenocarcinoma of lung Transitional cell carcinoma of the bladder Neoplasm Pancreatic adenocarcinoma Adenocarcinoma of stomach Malignant melanoma of skin Squamous cell carcinoma of the skin Hepatocellular carcinoma
Reversed	1
HGVS	NC_000009.11:g.21971111G>A; NC_000009.11:g.21971111G>C
CLNSRC
CLNACC	RCV000419112.1, RCV000421013.1, RCV000423848.1, RCV000426295.1, RCV000429387.1, RCV000432117.1, RCV000438754.1, RCV000438919.1, RCV000439424.1, RCV000418136.1, RCV000418718.1, RCV000425239.1, RCV000428114.1, RCV000428379.1, RCV000434935.1, RCV000436374.1, RCV000441259.1,