Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.35 (A)
Location

Chromosome 1:62837115 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs17388534

This variant has 3 HGVS names - click the plus to show

1:g.62837115A>G
ENST00000317868.8:c.1089+2263A>G
ENST00000371120.7:c.1089+2263A>G

Genotyping chips

This variant has assays on: Illumina_Cardio-Metabo_Chip

About this variant

This variant overlaps 3 transcripts, has 5094 sample genotypes, is associated with 1 phenotype and is mentioned in 1 citation.

Variant displays