rs2249077

Homo sapiens
T>C
SCLY : Intron Variant
UBE2F-SCLY : Intron Variant
Check p-value
SNV (Single Nucleotide Variation)
T==0127 (3817/29924,GnomAD)
T==0130 (3802/29118,TOPMED)
T==0149 (744/5008,1000G)
T==0176 (679/3854,ALSPAC)
T==0188 (698/3708,TWINSUK)
chr2:238082344 (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.238082344T>C
GRCh37.p13 chr 2NC_000002.11:g.238990985T>C

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
1000GenomesAfricanSub1322T=0.092C=0.908
1000GenomesAmericanSub694T=0.180C=0.820
1000GenomesEast AsianSub1008T=0.029C=0.971
1000GenomesEuropeSub1006T=0.162C=0.838
1000GenomesGlobalStudy-wide5008T=0.149C=0.851
1000GenomesSouth AsianSub978T=0.310C=0.690
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854T=0.176C=0.824
The Genome Aggregation DatabaseAfricanSub8716T=0.111C=0.889
The Genome Aggregation DatabaseAmericanSub834T=0.170C=0.830
The Genome Aggregation DatabaseEast AsianSub1620T=0.025C=0.975
The Genome Aggregation DatabaseEuropeSub18452T=0.142C=0.857
The Genome Aggregation DatabaseGlobalStudy-wide29924T=0.127C=0.872
The Genome Aggregation DatabaseOtherSub302T=0.100C=0.900
Trans-Omics for Precision MedicineGlobalStudy-wide29118T=0.130C=0.869
UK 10K study - TwinsTWIN COHORTStudy-wide3708T=0.188C=0.812
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
rs22490779.2E-05alcohol consumption23743675

eQTL of rs2249077 in Brain tissues (GTEx Analysis Release V7)

Position (v37) eGene GeneID Variant p-value TSS Tissue
Chr2:238990985SCLYENSG00000132330.12T>C7.8532e-1021455Cerebellum
Chr2:238990985SCLYENSG00000132330.12T>C2.8719e-421455Frontal_Cortex_BA9
Chr2:238990985SCLYENSG00000132330.12T>C1.0714e-821455Cortex
Chr2:238990985SCLYENSG00000132330.12T>C2.0850e-821455Cerebellar_Hemisphere
Chr2:238990985SCLYENSG00000132330.12T>C1.4177e-321455Caudate_basal_ganglia
Chr2:238990985SCLYENSG00000132330.12T>C7.2091e-421455Anterior_cingulate_cortex

meQTL of rs2249077 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 )
chr2238950342238950447E067-40538
chr2238951505238951913E067-39072
chr2238970839238970899E067-20086
chr2238990205238990255E067-730
chr2238990452238990751E067-234
chr2238970839238970899E068-20086
chr2239017313239017876E06826328
chr2238951505238951913E069-39072
chr2238970839238970899E069-20086
chr2238989790238989866E069-1119
chr2238989941238990032E069-953
chr2238990205238990255E069-730
chr2238970839238970899E070-20086
chr2238950342238950447E071-40538
chr2238951505238951913E071-39072
chr2238951961238952020E071-38965
chr2238970839238970899E071-20086
chr2238989247238989354E071-1631
chr2238989790238989866E071-1119
chr2238989941238990032E071-953
chr2238990205238990255E071-730
chr2238990452238990751E071-234
chr2239007116239007529E07116131
chr2239017176239017226E07126191
chr2239017313239017876E07126328
chr2238950342238950447E072-40538
chr2238989790238989866E072-1119
chr2238989941238990032E072-953
chr2238990205238990255E072-730
chr2238990452238990751E072-234
chr2239014417239014467E07223432
chr2239014951239015001E07223966
chr2238970839238970899E073-20086
chr2239014951239015001E07323966
chr2238950342238950447E074-40538
chr2238951505238951913E074-39072
chr2238989790238989866E074-1119
chr2238989941238990032E074-953
chr2238990452238990751E074-234
chr2239017313239017876E07426328
chr2238994008238994058E0813023
chr2238994372238994803E0813387
chr2238993565238993671E0822580
chr2238994008238994058E0823023










Promoter Annotation (GRCh37.p13)

Chromosome Start End Region Distance(-/+:Up/Downstream)
chr2238968700238970607E067-20378
chr2238968700238970607E068-20378
chr2238968700238970607E069-20378
chr2238968700238970607E070-20378
chr2238968700238970607E071-20378
chr2238968700238970607E072-20378
chr2238968700238970607E073-20378
chr2238968700238970607E074-20378
chr2238968700238970607E081-20378
chr2238968700238970607E082-20378