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rs2151280

From SNPedia

Orientationminus
Stabilizedminus
Make rs2151280(C;C)
Make rs2151280(C;T)
Make rs2151280(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position22034720
GeneCDKN2B-AS1
is asnp
is mentioned by
dbSNPrs2151280
ebirs2151280
HLIrs2151280
Exacrs2151280
Varsomers2151280
Maprs2151280
PheGenIrs2151280
hapmaprs2151280
1000 genomesrs2151280
hgdprs2151280
ensemblrs2151280
gopubmedrs2151280
geneviewrs2151280
scholarrs2151280
googlers2151280
pharmgkbrs2151280
gwascentralrs2151280
openSNPrs2151280
23andMers2151280
23andMe allrs2151280
SNP Nexus

SNPshotrs2151280
SNPdbers2151280
MSV3drs2151280
GWAS Ctlgrs2151280
GMAF0.4734
Max Magnitude
? (C;C) (C;T) (T;T) 28

23andMe blog rs2151280 G 1.19 Basal Cell Carcinoma

[PMID 19578363OA-icon.png] New common variants affecting susceptibility to basal cell carcinoma

OMIM613062
Desc
Variant
Relatedalso


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

GWAS snp
PMID [PMID 24403052OA-icon.png]
Trait Basal cell carcinoma
Title Germline sequence variants in TGM3 and RGS22 confer risk of basal cell carcinoma.
Risk Allele G
P-val 3E-10
Odds Ratio 1.20 [1.14-1.27]


[PMID 25874495] Long noncoding RNAs POLR2E rs3787016 C/T and HULC rs7763881 A/C polymorphisms are associated with decreased risk of esophageal cancer