rs34968276

Orientation

minus

Stabilized

minus

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

Make rs34968276(A;A)

Make rs34968276(A;C)

Reference

GRCh38.p7 38.3/150

Chromosome

9

Position

21971110

Gene

CDKN2A

is a	snp
is	mentioned by
dbSNP	rs34968276
dbSNP (classic)	rs34968276
ClinGen	rs34968276
ebi	rs34968276
HLI	rs34968276
Exac	rs34968276
Gnomad	rs34968276
Varsome	rs34968276
LitVar	rs34968276
Map	rs34968276
PheGenI	rs34968276
Biobank	rs34968276
1000 genomes	rs34968276
hgdp	rs34968276
ensembl	rs34968276
geneview	rs34968276
scholar	rs34968276
google	rs34968276
pharmgkb	rs34968276
gwascentral	rs34968276
openSNP	rs34968276
23andMe	rs34968276
SNPshot	rs34968276
SNPdbe	rs34968276
MSV3d	rs34968276
GWAS Ctlg	rs34968276

Max Magnitude

0

ClinVar
Risk	rs34968276(A;A) rs34968276(G;G)
Alt	rs34968276(A;A) rs34968276(G;G)
Reference	Rs34968276(C;C)
Significance	Probable-Pathogenic
Disease	Adenocarcinoma of stomach Malignant melanoma of skin Adenocarcinoma of lung Pancreatic adenocarcinoma Squamous cell carcinoma of the skin Transitional cell carcinoma of the bladder Hepatocellular carcinoma Squamous cell carcinoma of the head and neck Hereditary cancer-predisposing syndrome
Variation	info
Gene	CDKN2A
CLNDBN	Adenocarcinoma of stomach Malignant melanoma of skin Adenocarcinoma of lung Pancreatic adenocarcinoma Squamous cell carcinoma of the skin Transitional cell carcinoma of the bladder Hepatocellular carcinoma Squamous cell carcinoma of the head and neck Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000009.11:g.21971109G>C; NC_000009.11:g.21971109G>T
CLNSRC
CLNACC	RCV000422116.1, RCV000422956.1, RCV000423602.1, RCV000431254.1, RCV000432376.1, RCV000433889.1, RCV000441491.1, RCV000443430.1, RCV000493314.1,