rs7833054

Homo sapiens
A>G
EIF3H : Intron Variant
Check p-value
SNV (Single Nucleotide Variation)
A==0113 (3391/29962,GnomAD)
A==0082 (2408/29118,TOPMED)
A==0156 (779/5008,1000G)
A==0111 (427/3854,ALSPAC)
A==0109 (404/3708,TWINSUK)
chr8:116668792 (GRCh38.p7) (8q23.3)
AD
GWASdb2
1   publication(s)
See rs on genome
94 Enhancers around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 8NC_000008.11:g.116668792A>G
GRCh37.p13 chr 8NC_000008.10:g.117681031A>G

Gene: EIF3H, eukaryotic translation initiation factor 3 subunit H(minus strand)

Molecule type Change Amino acid[Codon] SO Term
EIF3H transcriptNM_003756.2:c.N/AIntron Variant

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322A=0.035G=0.965
1000GenomesAmericanSub694A=0.200G=0.800
1000GenomesEast AsianSub1008A=0.331G=0.669
1000GenomesEuropeSub1006A=0.106G=0.894
1000GenomesGlobalStudy-wide5008A=0.156G=0.844
1000GenomesSouth AsianSub978A=0.160G=0.840
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854A=0.111G=0.889
The Genome Aggregation DatabaseAfricanSub8720A=0.048G=0.952
The Genome Aggregation DatabaseAmericanSub838A=0.190G=0.810
The Genome Aggregation DatabaseEast AsianSub1614A=0.327G=0.673
The Genome Aggregation DatabaseEuropeSub18488A=0.120G=0.879
The Genome Aggregation DatabaseGlobalStudy-wide29962A=0.113G=0.886
The Genome Aggregation DatabaseOtherSub302A=0.200G=0.800
Trans-Omics for Precision MedicineGlobalStudy-wide29118A=0.082G=0.917
UK 10K study - TwinsTWIN COHORTStudy-wide3708A=0.109G=0.891
PMID Title Author Journal
21314694Genomewide association analysis of symptoms of alcohol dependence in the molecular genetics of schizophrenia (MGS2) control sample.Kendler KSAlcohol Clin Exp Res

P-Value

SNP ID p-value Traits Study
rs78330540.000482alcohol dependence21314694

eQTL of rs7833054 in Brain tissues (GTEx Analysis Release V7)

Position (v37) eGene GeneID Variant p-value TSS Tissue
There is no eQTL annotation for this SNP

meQTL of rs7833054 in Fetal Brain

Probe ID Position Gene beta p-value
There is no meQTL annotation for this SNP

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 )
chr8117662094117662307E067-18724
chr8117662439117662517E067-18514
chr8117669946117671238E067-9793
chr8117677177117677353E067-3678
chr8117677594117678247E067-2784
chr8117635682117636032E068-44999
chr8117650365117650445E068-30586
chr8117666897117667001E068-14030
chr8117669946117671238E068-9793
chr8117677594117678247E068-2784
chr8117696798117696866E06815767
chr8117696959117697104E06815928
chr8117702426117702923E06821395
chr8117703070117703229E06822039
chr8117703487117703622E06822456
chr8117721339117722642E06840308
chr8117722698117722751E06841667
chr8117726923117727041E06845892
chr8117727102117727334E06846071
chr8117727534117727611E06846503
chr8117727631117727774E06846600
chr8117647447117647950E069-33081
chr8117648027117648102E069-32929
chr8117648290117648400E069-32631
chr8117648538117648588E069-32443
chr8117648655117648849E069-32182
chr8117669946117671238E069-9793
chr8117677594117678247E069-2784
chr8117697432117699103E06916401
chr8117703070117703229E06922039
chr8117703487117703622E06922456
chr8117649842117649898E070-31133
chr8117667773117667848E070-13183
chr8117667892117667968E070-13063
chr8117669455117669561E070-11470
chr8117669593117669655E070-11376
chr8117669946117671238E070-9793
chr8117677594117678247E070-2784
chr8117635682117636032E071-44999
chr8117636225117636379E071-44652
chr8117647312117647369E071-33662
chr8117647447117647950E071-33081
chr8117669946117671238E071-9793
chr8117677177117677353E071-3678
chr8117677594117678247E071-2784
chr8117635682117636032E072-44999
chr8117647447117647950E072-33081
chr8117648655117648849E072-32182
chr8117649133117649225E072-31806
chr8117650167117650256E072-30775
chr8117650365117650445E072-30586
chr8117650457117650517E072-30514
chr8117666897117667001E072-14030
chr8117669946117671238E072-9793
chr8117677594117678247E072-2784
chr8117695566117695750E07214535
chr8117696103117696211E07215072
chr8117699242117699439E07218211
chr8117705823117705885E07224792
chr8117705954117706197E07224923
chr8117706229117706317E07225198
chr8117706321117706539E07225290
chr8117706653117706712E07225622
chr8117707680117708014E07226649
chr8117708144117708391E07227113
chr8117669946117671238E073-9793
chr8117708144117708391E07327113
chr8117650167117650256E074-30775
chr8117650365117650445E074-30586
chr8117650457117650517E074-30514
chr8117662094117662307E074-18724
chr8117665574117665691E074-15340
chr8117666897117667001E074-14030
chr8117667285117667362E074-13669
chr8117669946117671238E074-9793
chr8117677594117678247E074-2784
chr8117694239117694319E07413208
chr8117694469117694545E07413438
chr8117694588117694668E07413557
chr8117703070117703229E07422039
chr8117703487117703622E07422456
chr8117631072117631211E081-49820
chr8117631470117631525E081-49506
chr8117640574117640618E081-40413
chr8117641010117641150E081-39881
chr8117669113117669390E081-11641
chr8117669455117669561E081-11470
chr8117669593117669655E081-11376
chr8117677594117678247E081-2784
chr8117631072117631211E082-49820
chr8117640484117640555E082-40476
chr8117669946117671238E082-9793
chr8117677594117678247E082-2784
chr8117722698117722751E08241667