rs104894094

Orientation

minus

Stabilized

minus

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

Make rs104894094(G;T)

Make rs104894094(T;T)

Reference

GRCh38 38.1/141

Chromosome

9

Position

21971058

Gene

CDKN2A

is a	snp
is	mentioned by
dbSNP	rs104894094
dbSNP (classic)	rs104894094
ClinGen	rs104894094
ebi	rs104894094
HLI	rs104894094
Exac	rs104894094
Gnomad	rs104894094
Varsome	rs104894094
LitVar	rs104894094
Map	rs104894094
PheGenI	rs104894094
Biobank	rs104894094
1000 genomes	rs104894094
hgdp	rs104894094
ensembl	rs104894094
geneview	rs104894094
scholar	rs104894094
google	rs104894094
pharmgkb	rs104894094
gwascentral	rs104894094
openSNP	rs104894094
23andMe	rs104894094
SNPshot	rs104894094
SNPdbe	rs104894094
MSV3d	rs104894094
GWAS Ctlg	rs104894094

Max Magnitude

0

OMIM	600160
Desc
Variant	0005
Related	also

ClinVar
Risk	rs104894094(C;C) rs104894094(T;T)
Alt	rs104894094(C;C) rs104894094(T;T)
Reference	Rs104894094(G;G)
Significance	Other
Disease	Melanoma Melanoma-pancreatic cancer syndrome Hereditary cancer-predisposing syndrome Hereditary cutaneous melanoma not provided Cutaneous melanoma not specified
Variation	info
Gene	CDKN2A
CLNDBN	Melanoma, cutaneous malignant, susceptibility to, 2 Melanoma-pancreatic cancer syndrome Hereditary cancer-predisposing syndrome Hereditary cutaneous melanoma not provided Cutaneous melanoma not specified
Reversed	1
HGVS	NC_000009.11:g.21971057C>A; NC_000009.11:g.21971057C>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000010018.2, RCV000010019.2, RCV000115334.7, RCV000196633.3, RCV000212400.3, RCV000415140.1, RCV000196728.1, RCV000216848.1, RCV000481176.1,