rs104894098

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(A;T)	7	Pancreatic cancer/Melanoma Syndrome
(T;T)	0	common in complete genomics

Make rs104894098(A;A)

Reference

GRCh38 38.1/141

Chromosome

9

Position

21970982

Gene

CDKN2A

is a	snp
is	mentioned by
dbSNP	rs104894098
dbSNP (classic)	rs104894098
ClinGen	rs104894098
ebi	rs104894098
HLI	rs104894098
Exac	rs104894098
Gnomad	rs104894098
Varsome	rs104894098
LitVar	rs104894098
Map	rs104894098
PheGenI	rs104894098
Biobank	rs104894098
1000 genomes	rs104894098
hgdp	rs104894098
ensembl	rs104894098
geneview	rs104894098
scholar	rs104894098
google	rs104894098
pharmgkb	rs104894098
gwascentral	rs104894098
openSNP	rs104894098
23andMe	rs104894098
SNPshot	rs104894098
SNPdbe	rs104894098
MSV3d	rs104894098
GWAS Ctlg	rs104894098

Max Magnitude

7

OMIM	600160
Desc
Variant	0013
Related	also

ClinVar
Risk	rs104894098(A;A)
Alt	rs104894098(A;A)
Reference	Rs104894098(T;T)
Significance	Other
Disease	Melanoma Hereditary cancer-predisposing syndrome not provided Hereditary cutaneous melanoma
Variation	info
Gene	CDKN2A
CLNDBN	Melanoma, cutaneous malignant, susceptibility to, 2 Hereditary cancer-predisposing syndrome not provided Hereditary cutaneous melanoma
Reversed	1
HGVS	NC_000009.11:g.21970981A>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000010027.2, RCV000160413.5, RCV000212403.2, RCV000227154.2,