rs7023329

Orientation

plus

Stabilized

plus

Make rs7023329(A;A)

Make rs7023329(A;G)

Make rs7023329(G;G)

Reference

GRCh38 38.1/141

Chromosome

9

Position

21816529

Gene

MTAP

is a	snp
is	mentioned by
dbSNP	rs7023329
dbSNP (classic)	rs7023329
ClinGen	rs7023329
ebi	rs7023329
HLI	rs7023329
Exac	rs7023329
Gnomad	rs7023329
Varsome	rs7023329
LitVar	rs7023329
Map	rs7023329
PheGenI	rs7023329
Biobank	rs7023329
1000 genomes	rs7023329
hgdp	rs7023329
ensembl	rs7023329
geneview	rs7023329
scholar	rs7023329
google	rs7023329
pharmgkb	rs7023329
gwascentral	rs7023329
openSNP	rs7023329
23andMe	rs7023329
SNPshot	rs7023329
SNPdbe	rs7023329
MSV3d	rs7023329
GWAS Ctlg	rs7023329

GMAF

0.4752

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

23andMe blog rs7023329 A 1.18 Melanoma

GWAS snp
PMID	[PMID 19578364]
Trait	Melanoma
Title	Genome-wide association study identifies three loci associated with melanoma risk
Risk Allele	A
P-val	4E-7
Odds Ratio	1.18 [1.10-1.25]

OMIM	606933
Desc	TYROSINASE; TYR
Variant
Related	also

[PMID 20574843] Associations of 9p21 variants with cutaneous malignant melanoma, nevi, and pigmentation phenotypes in melanoma-prone families with and without CDKN2A mutations

OMIM	155601
Desc
Variant
Related	also

OMIM	601800
Desc
Variant
Related	also

OMIM	613099
Desc
Variant
Related	also

[PMID 22034633] Role of Noncoding RNA ANRIL in Genesis of Plexiform Neurofibromas in Neurofibromatosis Type 1

GWAS snp
PMID	[PMID 21983787]
Trait
Title	Genome-wide association study identifies three new melanoma susceptibility loci.
Risk Allele
P-val	7E-9
Odds Ratio	1.2000 None

[PMID 23361049] Common genetic variants in the 9p21 region and their associations with multiple tumours