rs10968666

Homo sapiens
A>G
LINGO2 : Intron Variant
LOC105376004 : Non Coding Transcript Variant
Check p-value
SNV (Single Nucleotide Variation)
G=0072 (2159/29916,GnomAD)
G=0092 (2685/29116,TOPMED)
G=0079 (397/5008,1000G)
G=0049 (188/3854,ALSPAC)
G=0056 (207/3708,TWINSUK)
chr9:28603942 (GRCh38.p7) (9p21.1)
AD
GWASdb2
1   publication(s)
See rs on genome
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 9NC_000009.12:g.28603942A>G
GRCh37.p13 chr 9NC_000009.11:g.28603940A>G

Gene: LINGO2, leucine rich repeat and Ig domain containing 2(minus strand)

Molecule type Change Amino acid[Codon] SO Term
LINGO2 transcript variant 2NM_001258282.1:c.N/AIntron Variant
LINGO2 transcript variant 1NM_152570.2:c.N/AIntron Variant
LINGO2 transcript variant X3XM_011517719.1:c.N/AIntron Variant
LINGO2 transcript variant X2XM_017014303.1:c.N/AIntron Variant
LINGO2 transcript variant X6XM_011517724.2:c.N/AGenic Upstream Transcript Variant
LINGO2 transcript variant X7XM_011517728.2:c.N/AGenic Upstream Transcript Variant
LINGO2 transcript variant X3XM_017014304.1:c.N/AGenic Upstream Transcript Variant
LINGO2 transcript variant X4XM_017014305.1:c.N/AGenic Upstream Transcript Variant
LINGO2 transcript variant X6XM_017014306.1:c.N/AGenic Upstream Transcript Variant
LINGO2 transcript variant X8XM_017014307.1:c.N/AGenic Upstream Transcript Variant
LINGO2 transcript variant X1XR_001746186.1:n.N/AIntron Variant

Gene: LOC105376004, uncharacterized LOC105376004(plus strand)

Molecule type Change Amino acid[Codon] SO Term
LOC105376004 transcript variant X1XR_001746641.1:n....XR_001746641.1:n.5904A>GA>GNon Coding Transcript Variant
LOC105376004 transcript variant X2XR_929534.2:n.412...XR_929534.2:n.4128A>GA>GNon Coding Transcript Variant

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322A=0.831G=0.169
1000GenomesAmericanSub694A=0.940G=0.060
1000GenomesEast AsianSub1008A=0.963G=0.037
1000GenomesEuropeSub1006A=0.941G=0.059
1000GenomesGlobalStudy-wide5008A=0.921G=0.079
1000GenomesSouth AsianSub978A=0.960G=0.040
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854A=0.951G=0.049
The Genome Aggregation DatabaseAfricanSub8708A=0.864G=0.136
The Genome Aggregation DatabaseAmericanSub834A=0.950G=0.050
The Genome Aggregation DatabaseEast AsianSub1618A=0.972G=0.028
The Genome Aggregation DatabaseEuropeSub18454A=0.952G=0.047
The Genome Aggregation DatabaseGlobalStudy-wide29916A=0.927G=0.072
The Genome Aggregation DatabaseOtherSub302A=0.960G=0.040
Trans-Omics for Precision MedicineGlobalStudy-wide29116A=0.907G=0.092
UK 10K study - TwinsTWIN COHORTStudy-wide3708A=0.944G=0.056
PMID Title Author Journal
24962325Genome-wide survival analysis of age at onset of alcohol dependence in extended high-risk COGA families.Kapoor MDrug Alcohol Depend

P-Value

SNP ID p-value Traits Study
rs109686662.29E-06alcohol dependence (age at onset)24962325

eQTL of rs10968666 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 rs10968666 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 )
chr92856335728563890E067-40050
chr92859848828598755E067-5185
chr92859883428598942E067-4998
chr92859896828599094E067-4846
chr92859910028599299E067-4641
chr92860004728600170E067-3770
chr92860021028600634E067-3306
chr92860069628600780E067-3160
chr92860079528600835E067-3105
chr92860109228601325E067-2615
chr92856335728563890E069-40050
chr92859710228597684E069-6256
chr92859830328598375E069-5565
chr92859848828598755E069-5185
chr92859883428598942E069-4998
chr92859896828599094E069-4846
chr92859910028599299E069-4641
chr92859830328598375E070-5565
chr92860004728600170E070-3770
chr92860021028600634E070-3306
chr92860069628600780E070-3160
chr92860079528600835E070-3105
chr92860109228601325E070-2615
chr92860144228601609E070-2331
chr92860221628602266E070-1674
chr92860258728602672E070-1268
chr92860273628603213E070-727
chr92856335728563890E071-40050
chr92859848828598755E071-5185
chr92860021028600634E071-3306
chr92860069628600780E071-3160
chr92860079528600835E071-3105
chr92860109228601325E071-2615
chr92860144228601609E071-2331
chr92860221628602266E071-1674
chr92860258728602672E071-1268
chr92859848828598755E072-5185
chr92856310228563191E081-40749
chr92860144228601609E082-2331