rs2262426

Homo sapiens
G>A
SCLY : Intron Variant
UBE2F-SCLY : Intron Variant
Check p-value
SNV (Single Nucleotide Variation)
G==0127 (3811/29878,GnomAD)
G==0129 (3776/29118,TOPMED)
G==0149 (745/5008,1000G)
G==0176 (679/3854,ALSPAC)
G==0189 (699/3708,TWINSUK)
chr2:238075856 (GRCh38.p7) (2q37.3)
AD
GWASdb2
1   publication(s)
See rs on genome

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 2NC_000002.12:g.238075856G>A
GRCh37.p13 chr 2NC_000002.11:g.238984497G>A

Gene: SCLY, selenocysteine lyase(plus strand)

Molecule type Change Amino acid[Codon] SO Term
SCLY transcriptNM_016510.5:c.N/AIntron Variant

Gene: UBE2F-SCLY, UBE2F-SCLY readthrough (NMD candidate)(plus strand)

Molecule type Change Amino acid[Codon] SO Term
UBE2F-SCLY transcriptNR_037904.1:n.N/AIntron Variant

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322G=0.092A=0.908
1000GenomesAmericanSub694G=0.180A=0.820
1000GenomesEast AsianSub1008G=0.029A=0.971
1000GenomesEuropeSub1006G=0.162A=0.838
1000GenomesGlobalStudy-wide5008G=0.149A=0.851
1000GenomesSouth AsianSub978G=0.310A=0.690
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854G=0.176A=0.824
The Genome Aggregation DatabaseAfricanSub8720G=0.110A=0.890
The Genome Aggregation DatabaseAmericanSub838G=0.170A=0.830
The Genome Aggregation DatabaseEast AsianSub1620G=0.025A=0.975
The Genome Aggregation DatabaseEuropeSub18400G=0.143A=0.856
The Genome Aggregation DatabaseGlobalStudy-wide29878G=0.127A=0.872
The Genome Aggregation DatabaseOtherSub300G=0.100A=0.900
Trans-Omics for Precision MedicineGlobalStudy-wide29118G=0.129A=0.870
UK 10K study - TwinsTWIN COHORTStudy-wide3708G=0.189A=0.811
PMID Title Author Journal
23743675A meta-analysis of two genome-wide association studies to identify novel loci for maximum number of alcoholic drinks.Kapoor MHum Genet

P-Value

SNP ID p-value Traits Study
rs22624260.000133alcohol consumption23743675

eQTL of rs2262426 in Brain tissues (GTEx Analysis Release V7)

Position (v37) eGene GeneID Variant p-value TSS Tissue
Chr2:238984497SCLYENSG00000132330.12G>A7.8532e-1014967Cerebellum
Chr2:238984497SCLYENSG00000132330.12G>A2.8719e-414967Frontal_Cortex_BA9
Chr2:238984497SCLYENSG00000132330.12G>A1.0714e-814967Cortex
Chr2:238984497SCLYENSG00000132330.12G>A2.0850e-814967Cerebellar_Hemisphere
Chr2:238984497SCLYENSG00000132330.12G>A1.4177e-314967Caudate_basal_ganglia
Chr2:238984497SCLYENSG00000132330.12G>A2.3006e-314967Substantia_nigra
Chr2:238984497SCLYENSG00000132330.12G>A7.2091e-414967Anterior_cingulate_cortex

meQTL of rs2262426 in Fetal Brain

Probe ID Position Gene beta p-value
cg03558837chr2:239029375ESPNL0.06462263479058882.4442e-14

Genomic View

Chromatin Interaction

There is no significant Hi-C chromatin interaction data for this SNP.

Enhancer Annotation (GRCh37.p13)

Chromosome Start End Region Distance ( -/+ : Up/Downstream )
chr2238950342238950447E067-34050
chr2238951505238951913E067-32584
chr2238970839238970899E067-13598
chr2238990205238990255E0675708
chr2238990452238990751E0675955
chr2238970839238970899E068-13598
chr2239017313239017876E06832816
chr2238951505238951913E069-32584
chr2238970839238970899E069-13598
chr2238989790238989866E0695293
chr2238989941238990032E0695444
chr2238990205238990255E0695708
chr2238970839238970899E070-13598
chr2238950342238950447E071-34050
chr2238951505238951913E071-32584
chr2238951961238952020E071-32477
chr2238970839238970899E071-13598
chr2238989247238989354E0714750
chr2238989790238989866E0715293
chr2238989941238990032E0715444
chr2238990205238990255E0715708
chr2238990452238990751E0715955
chr2239007116239007529E07122619
chr2239017176239017226E07132679
chr2239017313239017876E07132816
chr2238950342238950447E072-34050
chr2238989790238989866E0725293
chr2238989941238990032E0725444
chr2238990205238990255E0725708
chr2238990452238990751E0725955
chr2239014417239014467E07229920
chr2239014951239015001E07230454
chr2238970839238970899E073-13598
chr2239014951239015001E07330454
chr2238950342238950447E074-34050
chr2238951505238951913E074-32584
chr2238989790238989866E0745293
chr2238989941238990032E0745444
chr2238990452238990751E0745955
chr2239017313239017876E07432816
chr2238994008238994058E0819511
chr2238994372238994803E0819875
chr2238993565238993671E0829068
chr2238994008238994058E0829511










Promoter Annotation (GRCh37.p13)

Chromosome Start End Region Distance(-/+:Up/Downstream)
chr2238968700238970607E067-13890
chr2238968700238970607E068-13890
chr2238968700238970607E069-13890
chr2238968700238970607E070-13890
chr2238968700238970607E071-13890
chr2238968700238970607E072-13890
chr2238968700238970607E073-13890
chr2238968700238970607E074-13890
chr2238968700238970607E081-13890
chr2238968700238970607E082-13890