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rs10757257

From SNPedia

Orientationplus
Stabilizedplus
Make rs10757257(A;A)
Make rs10757257(A;G)
Make rs10757257(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position21806565
GeneMTAP
is asnp
is mentioned by
dbSNPrs10757257
ebirs10757257
HLIrs10757257
Exacrs10757257
Varsomers10757257
Maprs10757257
PheGenIrs10757257
hapmaprs10757257
1000 genomesrs10757257
hgdprs10757257
ensemblrs10757257
gopubmedrs10757257
geneviewrs10757257
scholarrs10757257
googlers10757257
pharmgkbrs10757257
gwascentralrs10757257
openSNPrs10757257
23andMers10757257
23andMe allrs10757257
SNP Nexus

SNPshotrs10757257
SNPdbers10757257
MSV3drs10757257
GWAS Ctlgrs10757257
GMAF0.3466
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 19578365OA-icon.png] Genome-wide association study identifies variants at 9p21 and 22q13 associated with development of cutaneous nevi
OMIM155601
Desc
Variant
Relatedalso
OMIM162900
Desc
Variant
Relatedalso


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


[PMID 19578364OA-icon.png] Genome-wide association study identifies three loci associated with melanoma risk.


[PMID 21962134OA-icon.png] Polymorphisms in nevus-associated genes MTAP, PLA2G6, and IRF4 and the risk of invasive cutaneous melanoma.