Have questions? Visit https://www.reddit.com/r/SNPedia

rs7023329

From SNPedia

Orientationplus
Stabilizedplus
Make rs7023329(A;A)
Make rs7023329(A;G)
Make rs7023329(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position21816529
GeneMTAP
is asnp
is mentioned by
dbSNPrs7023329
ebirs7023329
HLIrs7023329
Exacrs7023329
Varsomers7023329
Maprs7023329
PheGenIrs7023329
hapmaprs7023329
1000 genomesrs7023329
hgdprs7023329
ensemblrs7023329
gopubmedrs7023329
geneviewrs7023329
scholarrs7023329
googlers7023329
pharmgkbrs7023329
gwascentralrs7023329
openSNPrs7023329
23andMers7023329
23andMe allrs7023329
SNP Nexus

SNPshotrs7023329
SNPdbers7023329
MSV3drs7023329
GWAS Ctlgrs7023329
GMAF0.4752
Max Magnitude
? (A;A) (A;G) (G;G) 28
23andMe blog rs7023329 A 1.18 Melanoma
GWAS snp
PMID [PMID 19578364OA-icon.png]
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]
OMIM606933
DescTYROSINASE; TYR
Variant
Relatedalso
[PMID 20574843OA-icon.png] Associations of 9p21 variants with cutaneous malignant melanoma, nevi, and pigmentation phenotypes in melanoma-prone families with and without CDKN2A mutations
OMIM155601
Desc
Variant
Relatedalso
OMIM601800
Desc
Variant
Relatedalso
OMIM613099
Desc
Variant
Relatedalso


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

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


GET Evidence
rs7023329
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.5
summary



[PMID 23361049OA-icon.png] Common genetic variants in the 9p21 region and their associations with multiple tumours