rs104894095

Orientation

minus

Stabilized

minus

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

Make rs104894095(C;C)

Make rs104894095(C;G)

Reference

GRCh38 38.1/141

Chromosome

9

Position

21971200

Gene

CDKN2A

is a	snp
is	mentioned by
dbSNP	rs104894095
dbSNP (classic)	rs104894095
ClinGen	rs104894095
ebi	rs104894095
HLI	rs104894095
Exac	rs104894095
Gnomad	rs104894095
Varsome	rs104894095
LitVar	rs104894095
Map	rs104894095
PheGenI	rs104894095
Biobank	rs104894095
1000 genomes	rs104894095
hgdp	rs104894095
ensembl	rs104894095
geneview	rs104894095
scholar	rs104894095
google	rs104894095
pharmgkb	rs104894095
gwascentral	rs104894095
openSNP	rs104894095
23andMe	rs104894095
SNPshot	rs104894095
SNPdbe	rs104894095
MSV3d	rs104894095
GWAS Ctlg	rs104894095

Max Magnitude

0

OMIM	600160
Desc
Variant	0007
Related	also

ClinVar
Risk	rs104894095(A;A) rs104894095(C;C)
Alt	rs104894095(A;A) rs104894095(C;C)
Reference	Rs104894095(G;G)
Significance	Other
Disease	Melanoma Hereditary cancer-predisposing syndrome Hereditary cutaneous melanoma not provided
Variation	info
Gene	CDKN2A
CLNDBN	Melanoma, cutaneous malignant, susceptibility to, 2 Hereditary cancer-predisposing syndrome Hereditary cutaneous melanoma not provided
Reversed	1
HGVS	NC_000009.11:g.21971199C>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000010021.2, RCV000160421.4, RCV000205342.2, RCV000212399.3,