rs4663836

Homo sapiens
A>T
SCLY : Intron Variant
UBE2F-SCLY : Intron Variant
Check p-value
SNV (Single Nucleotide Variation)
A==0125 (3750/29964,GnomAD)
A==0126 (3694/29118,TOPMED)
A==0147 (734/5008,1000G)
A==0176 (679/3854,ALSPAC)
A==0189 (699/3708,TWINSUK)
chr2:238078544 (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.238078544A>T
GRCh37.p13 chr 2NC_000002.11:g.238987185A>T

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
1000GenomesAfricanSub1322A=0.083T=0.917
1000GenomesAmericanSub694A=0.180T=0.820
1000GenomesEast AsianSub1008A=0.029T=0.971
1000GenomesEuropeSub1006A=0.162T=0.838
1000GenomesGlobalStudy-wide5008A=0.147T=0.853
1000GenomesSouth AsianSub978A=0.310T=0.690
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854A=0.176T=0.824
The Genome Aggregation DatabaseAfricanSub8726A=0.102T=0.898
The Genome Aggregation DatabaseAmericanSub838A=0.170T=0.830
The Genome Aggregation DatabaseEast AsianSub1622A=0.025T=0.975
The Genome Aggregation DatabaseEuropeSub18476A=0.143T=0.856
The Genome Aggregation DatabaseGlobalStudy-wide29964A=0.125T=0.874
The Genome Aggregation DatabaseOtherSub302A=0.100T=0.900
Trans-Omics for Precision MedicineGlobalStudy-wide29118A=0.126T=0.873
UK 10K study - TwinsTWIN COHORTStudy-wide3708A=0.189T=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
rs46638369.6E-05alcohol consumption23743675

eQTL of rs4663836 in Brain tissues (GTEx Analysis Release V7)

Position (v37) eGene GeneID Variant p-value TSS Tissue
Chr2:238987185SCLYENSG00000132330.12A>T7.8532e-1017655Cerebellum
Chr2:238987185SCLYENSG00000132330.12A>T2.8719e-417655Frontal_Cortex_BA9
Chr2:238987185SCLYENSG00000132330.12A>T1.0714e-817655Cortex
Chr2:238987185SCLYENSG00000132330.12A>T2.0850e-817655Cerebellar_Hemisphere
Chr2:238987185SCLYENSG00000132330.12A>T7.2091e-417655Anterior_cingulate_cortex

meQTL of rs4663836 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 )
chr2238950342238950447E067-36738
chr2238951505238951913E067-35272
chr2238970839238970899E067-16286
chr2238990205238990255E0673020
chr2238990452238990751E0673267
chr2238970839238970899E068-16286
chr2239017313239017876E06830128
chr2238951505238951913E069-35272
chr2238970839238970899E069-16286
chr2238989790238989866E0692605
chr2238989941238990032E0692756
chr2238990205238990255E0693020
chr2238970839238970899E070-16286
chr2238950342238950447E071-36738
chr2238951505238951913E071-35272
chr2238951961238952020E071-35165
chr2238970839238970899E071-16286
chr2238989247238989354E0712062
chr2238989790238989866E0712605
chr2238989941238990032E0712756
chr2238990205238990255E0713020
chr2238990452238990751E0713267
chr2239007116239007529E07119931
chr2239017176239017226E07129991
chr2239017313239017876E07130128
chr2238950342238950447E072-36738
chr2238989790238989866E0722605
chr2238989941238990032E0722756
chr2238990205238990255E0723020
chr2238990452238990751E0723267
chr2239014417239014467E07227232
chr2239014951239015001E07227766
chr2238970839238970899E073-16286
chr2239014951239015001E07327766
chr2238950342238950447E074-36738
chr2238951505238951913E074-35272
chr2238989790238989866E0742605
chr2238989941238990032E0742756
chr2238990452238990751E0743267
chr2239017313239017876E07430128
chr2238994008238994058E0816823
chr2238994372238994803E0817187
chr2238993565238993671E0826380
chr2238994008238994058E0826823










Promoter Annotation (GRCh37.p13)

Chromosome Start End Region Distance(-/+:Up/Downstream)
chr2238968700238970607E067-16578
chr2238968700238970607E068-16578
chr2238968700238970607E069-16578
chr2238968700238970607E070-16578
chr2238968700238970607E071-16578
chr2238968700238970607E072-16578
chr2238968700238970607E073-16578
chr2238968700238970607E074-16578
chr2238968700238970607E081-16578
chr2238968700238970607E082-16578