rs104894099

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(T;T)	0	common in complete genomics

Make rs104894099(G;G)

Make rs104894099(G;T)

Reference

GRCh38 38.1/141

Chromosome

9

Position

21971183

Gene

CDKN2A

is a	snp
is	mentioned by
dbSNP	rs104894099
dbSNP (classic)	rs104894099
ClinGen	rs104894099
ebi	rs104894099
HLI	rs104894099
Exac	rs104894099
Gnomad	rs104894099
Varsome	rs104894099
LitVar	rs104894099
Map	rs104894099
PheGenI	rs104894099
Biobank	rs104894099
1000 genomes	rs104894099
hgdp	rs104894099
ensembl	rs104894099
geneview	rs104894099
scholar	rs104894099
google	rs104894099
pharmgkb	rs104894099
gwascentral	rs104894099
openSNP	rs104894099
23andMe	rs104894099
SNPshot	rs104894099
SNPdbe	rs104894099
MSV3d	rs104894099
GWAS Ctlg	rs104894099

Max Magnitude

0

OMIM	600160
Desc
Variant	0016
Related	also

ClinVar
Risk	rs104894099(G;G)
Alt	rs104894099(G;G)
Reference	Rs104894099(T;T)
Significance	Other
Disease	Melanoma Melanoma-pancreatic cancer syndrome Hereditary cancer-predisposing syndrome
Variation	info
Gene	CDKN2A
CLNDBN	Melanoma, cutaneous malignant, susceptibility to, 2 Melanoma-pancreatic cancer syndrome Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000009.11:g.21971182A>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000010030.2, RCV000409228.1, RCV000494082.1,