rs7601010

Homo sapiens
C>T
SCLY : Intron Variant
UBE2F-SCLY : Intron Variant
Check p-value
SNV (Single Nucleotide Variation)
C==0127 (3816/29904,GnomAD)
C==0130 (3798/29118,TOPMED)
C==0149 (747/5008,1000G)
C==0176 (678/3854,ALSPAC)
C==0189 (700/3708,TWINSUK)
chr2:238074132 (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.238074132C>T
GRCh37.p13 chr 2NC_000002.11:g.238982773C>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
1000GenomesAfricanSub1322C=0.093T=0.907
1000GenomesAmericanSub694C=0.180T=0.820
1000GenomesEast AsianSub1008C=0.029T=0.971
1000GenomesEuropeSub1006C=0.162T=0.838
1000GenomesGlobalStudy-wide5008C=0.149T=0.851
1000GenomesSouth AsianSub978C=0.310T=0.690
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854C=0.176T=0.824
The Genome Aggregation DatabaseAfricanSub8692C=0.111T=0.889
The Genome Aggregation DatabaseAmericanSub838C=0.170T=0.830
The Genome Aggregation DatabaseEast AsianSub1618C=0.025T=0.975
The Genome Aggregation DatabaseEuropeSub18454C=0.143T=0.857
The Genome Aggregation DatabaseGlobalStudy-wide29904C=0.127T=0.872
The Genome Aggregation DatabaseOtherSub302C=0.100T=0.900
Trans-Omics for Precision MedicineGlobalStudy-wide29118C=0.130T=0.869
UK 10K study - TwinsTWIN COHORTStudy-wide3708C=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
rs76010100.000144alcohol consumption23743675

eQTL of rs7601010 in Brain tissues (GTEx Analysis Release V7)

Position (v37) eGene GeneID Variant p-value TSS Tissue
Chr2:238982773SCLYENSG00000132330.12C>T7.8532e-1013243Cerebellum
Chr2:238982773SCLYENSG00000132330.12C>T2.8719e-413243Frontal_Cortex_BA9
Chr2:238982773SCLYENSG00000132330.12C>T1.0714e-813243Cortex
Chr2:238982773SCLYENSG00000132330.12C>T2.0850e-813243Cerebellar_Hemisphere
Chr2:238982773SCLYENSG00000132330.12C>T1.4177e-313243Caudate_basal_ganglia
Chr2:238982773SCLYENSG00000132330.12C>T7.2091e-413243Anterior_cingulate_cortex

meQTL of rs7601010 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 )
chr2238950342238950447E067-32326
chr2238951505238951913E067-30860
chr2238970839238970899E067-11874
chr2238990205238990255E0677432
chr2238990452238990751E0677679
chr2238970839238970899E068-11874
chr2239017313239017876E06834540
chr2238951505238951913E069-30860
chr2238970839238970899E069-11874
chr2238989790238989866E0697017
chr2238989941238990032E0697168
chr2238990205238990255E0697432
chr2238970839238970899E070-11874
chr2238950342238950447E071-32326
chr2238951505238951913E071-30860
chr2238951961238952020E071-30753
chr2238970839238970899E071-11874
chr2238989247238989354E0716474
chr2238989790238989866E0717017
chr2238989941238990032E0717168
chr2238990205238990255E0717432
chr2238990452238990751E0717679
chr2239007116239007529E07124343
chr2239017176239017226E07134403
chr2239017313239017876E07134540
chr2238950342238950447E072-32326
chr2238989790238989866E0727017
chr2238989941238990032E0727168
chr2238990205238990255E0727432
chr2238990452238990751E0727679
chr2239014417239014467E07231644
chr2239014951239015001E07232178
chr2238970839238970899E073-11874
chr2239014951239015001E07332178
chr2238950342238950447E074-32326
chr2238951505238951913E074-30860
chr2238989790238989866E0747017
chr2238989941238990032E0747168
chr2238990452238990751E0747679
chr2239017313239017876E07434540
chr2238994008238994058E08111235
chr2238994372238994803E08111599
chr2238993565238993671E08210792
chr2238994008238994058E08211235










Promoter Annotation (GRCh37.p13)

Chromosome Start End Region Distance(-/+:Up/Downstream)
chr2238968700238970607E067-12166
chr2238968700238970607E068-12166
chr2238968700238970607E069-12166
chr2238968700238970607E070-12166
chr2238968700238970607E071-12166
chr2238968700238970607E072-12166
chr2238968700238970607E073-12166
chr2238968700238970607E074-12166
chr2238968700238970607E081-12166
chr2238968700238970607E082-12166