rs16842733

Homo sapiens
A>G
NEK7 : Intron Variant
Check p-value
SNV (Single Nucleotide Variation)
G=0078 (2346/29926,GnomAD)
G=0087 (2544/29118,TOPMED)
G=0109 (546/5008,1000G)
G=0038 (148/3854,ALSPAC)
G=0039 (143/3708,TWINSUK)
chr1:198304970 (GRCh38.p7) (1q31.3)
ND
GWASdb2
1   publication(s)
See rs on genome
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 1NC_000001.11:g.198304970A>G
GRCh37.p13 chr 1NC_000001.10:g.198274100A>G

Gene: NEK7, NIMA related kinase 7(plus strand)

Molecule type Change Amino acid[Codon] SO Term
NEK7 transcriptNM_133494.2:c.N/AIntron Variant
NEK7 transcript variant X6XM_011509209.1:c.N/AIntron Variant
NEK7 transcript variant X1XM_017000344.1:c.N/AIntron Variant
NEK7 transcript variant X2XM_017000345.1:c.N/AIntron Variant
NEK7 transcript variant X3XM_017000346.1:c.N/AIntron Variant
NEK7 transcript variant X4XM_017000347.1:c.N/AGenic Downstream Transcript Variant
NEK7 transcript variant X5XM_017000348.1:c.N/AGenic Downstream Transcript Variant

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322A=0.889G=0.111
1000GenomesAmericanSub694A=0.870G=0.130
1000GenomesEast AsianSub1008A=0.820G=0.180
1000GenomesEuropeSub1006A=0.956G=0.044
1000GenomesGlobalStudy-wide5008A=0.891G=0.109
1000GenomesSouth AsianSub978A=0.910G=0.090
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854A=0.962G=0.038
The Genome Aggregation DatabaseAfricanSub8726A=0.884G=0.116
The Genome Aggregation DatabaseAmericanSub838A=0.800G=0.200
The Genome Aggregation DatabaseEast AsianSub1616A=0.858G=0.142
The Genome Aggregation DatabaseEuropeSub18444A=0.950G=0.049
The Genome Aggregation DatabaseGlobalStudy-wide29926A=0.921G=0.078
The Genome Aggregation DatabaseOtherSub302A=0.940G=0.060
Trans-Omics for Precision MedicineGlobalStudy-wide29118A=0.912G=0.087
UK 10K study - TwinsTWIN COHORTStudy-wide3708A=0.961G=0.039
PMID Title Author Journal
17158188Novel genes identified in a high-density genome wide association study for nicotine dependence.Bierut LJHum Mol Genet

P-Value

SNP ID p-value Traits Study
rs168427330.000442nicotine dependence17158188

eQTL of rs16842733 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 rs16842733 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 )
chr1198234177198234919E067-39181
chr1198265159198265390E067-8710
chr1198285283198285333E06711183
chr1198286417198286550E06712317
chr1198234177198234919E068-39181
chr1198264401198264696E068-9404
chr1198265159198265390E068-8710
chr1198234177198234919E069-39181
chr1198273569198273879E069-221
chr1198285283198285333E06911183
chr1198245499198245631E070-28469
chr1198245734198245788E070-28312
chr1198265159198265390E070-8710
chr1198267867198268155E070-5945
chr1198285881198286086E07011781
chr1198286417198286550E07012317
chr1198287370198287455E07013270
chr1198237858198238218E071-35882
chr1198238244198239007E071-35093
chr1198264401198264696E071-9404
chr1198273569198273879E071-221
chr1198234177198234919E072-39181
chr1198238244198239007E072-35093
chr1198273569198273879E072-221
chr1198285283198285333E07211183
chr1198285881198286086E07211781
chr1198286417198286550E07212317
chr1198234177198234919E073-39181
chr1198234177198234919E074-39181
chr1198237627198237687E074-36413
chr1198237858198238218E074-35882
chr1198285881198286086E07411781
chr1198286417198286550E07412317
chr1198257408198257532E081-16568
chr1198264401198264696E081-9404
chr1198265159198265390E081-8710
chr1198267867198268155E081-5945
chr1198302038198302078E08127938
chr1198256992198257340E082-16760
chr1198257408198257532E082-16568
chr1198265159198265390E082-8710
chr1198267867198268155E082-5945