rs2249067

Homo sapiens
G>A
SCLY : Intron Variant
UBE2F-SCLY : Intron Variant
Check p-value
SNV (Single Nucleotide Variation)
G==0124 (3733/29944,GnomAD)
G==0126 (3673/29118,TOPMED)
G==0146 (733/5008,1000G)
G==0176 (680/3854,ALSPAC)
G==0188 (698/3708,TWINSUK)
chr2:238082546 (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.238082546G>A
GRCh37.p13 chr 2NC_000002.11:g.238991187G>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=0.083A=0.917
1000GenomesAmericanSub694G=0.180A=0.820
1000GenomesEast AsianSub1008G=0.029A=0.971
1000GenomesEuropeSub1006G=0.162A=0.838
1000GenomesGlobalStudy-wide5008G=0.146A=0.854
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 DatabaseAfricanSub8712G=0.100A=0.900
The Genome Aggregation DatabaseAmericanSub838G=0.170A=0.830
The Genome Aggregation DatabaseEast AsianSub1618G=0.024A=0.976
The Genome Aggregation DatabaseEuropeSub18474G=0.143A=0.856
The Genome Aggregation DatabaseGlobalStudy-wide29944G=0.124A=0.875
The Genome Aggregation DatabaseOtherSub302G=0.100A=0.900
Trans-Omics for Precision MedicineGlobalStudy-wide29118G=0.126A=0.873
UK 10K study - TwinsTWIN COHORTStudy-wide3708G=0.188A=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
rs22490676.89E-05alcohol consumption23743675

eQTL of rs2249067 in Brain tissues (GTEx Analysis Release V7)

Position (v37) eGene GeneID Variant p-value TSS Tissue
Chr2:238991187SCLYENSG00000132330.12G>A7.8532e-1021657Cerebellum
Chr2:238991187SCLYENSG00000132330.12G>A2.8719e-421657Frontal_Cortex_BA9
Chr2:238991187SCLYENSG00000132330.12G>A1.0714e-821657Cortex
Chr2:238991187SCLYENSG00000132330.12G>A2.0850e-821657Cerebellar_Hemisphere
Chr2:238991187SCLYENSG00000132330.12G>A1.4177e-321657Caudate_basal_ganglia
Chr2:238991187SCLYENSG00000132330.12G>A7.2091e-421657Anterior_cingulate_cortex

meQTL of rs2249067 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 )
chr2238950342238950447E067-40740
chr2238951505238951913E067-39274
chr2238970839238970899E067-20288
chr2238990205238990255E067-932
chr2238990452238990751E067-436
chr2238970839238970899E068-20288
chr2239017313239017876E06826126
chr2238951505238951913E069-39274
chr2238970839238970899E069-20288
chr2238989790238989866E069-1321
chr2238989941238990032E069-1155
chr2238990205238990255E069-932
chr2238970839238970899E070-20288
chr2238950342238950447E071-40740
chr2238951505238951913E071-39274
chr2238951961238952020E071-39167
chr2238970839238970899E071-20288
chr2238989247238989354E071-1833
chr2238989790238989866E071-1321
chr2238989941238990032E071-1155
chr2238990205238990255E071-932
chr2238990452238990751E071-436
chr2239007116239007529E07115929
chr2239017176239017226E07125989
chr2239017313239017876E07126126
chr2238950342238950447E072-40740
chr2238989790238989866E072-1321
chr2238989941238990032E072-1155
chr2238990205238990255E072-932
chr2238990452238990751E072-436
chr2239014417239014467E07223230
chr2239014951239015001E07223764
chr2238970839238970899E073-20288
chr2239014951239015001E07323764
chr2238950342238950447E074-40740
chr2238951505238951913E074-39274
chr2238989790238989866E074-1321
chr2238989941238990032E074-1155
chr2238990452238990751E074-436
chr2239017313239017876E07426126
chr2238994008238994058E0812821
chr2238994372238994803E0813185
chr2238993565238993671E0822378
chr2238994008238994058E0822821










Promoter Annotation (GRCh37.p13)

Chromosome Start End Region Distance(-/+:Up/Downstream)
chr2238968700238970607E067-20580
chr2238968700238970607E068-20580
chr2238968700238970607E069-20580
chr2238968700238970607E070-20580
chr2238968700238970607E071-20580
chr2238968700238970607E072-20580
chr2238968700238970607E073-20580
chr2238968700238970607E074-20580
chr2238968700238970607E081-20580
chr2238968700238970607E082-20580