Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.21 (A)
Location

Chromosome 2:60493816 (forward strand) | View in location tab

Co-located
Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs52835308, rs118120356

This variant has 9 HGVS names - click the plus to show

2:g.60493816A>G
ENST00000356842.8:c.386-24983T>C
ENST00000492272.5:n.228-24983T>C
ENST00000631857.1:c.*100+14790T>C
ENST00000335712.10:c.386-24983T>C
ENST00000359629.9:c.386-24983T>C
ENST00000477659.1:n.69-24983T>C
ENST00000489516.6:c.230-24983T>C
ENST00000358510.5:c.386-31392T>C

Genotyping chips

This variant has assays on: Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 9 transcripts, has 2818 sample genotypes, is associated with 1 phenotype and is mentioned in 26 citations.

Variant displays