Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

G/A | Ancestral: G | Ambiguity code: R | MAF: 0.14 (A)

Chromosome 13:113118393 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs36209565, rs59860661

HGVS names

This variant has 4 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_HumanOmni1-Quad, Illumina_HumanOmni5

About this variant

This variant overlaps 12 transcripts, has 3671 sample genotypes, is associated with 1 phenotype and is mentioned in 1 citation.

Variant displays