Original source

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

A/C/G | Ancestral: A | Ambiguity code: V | MAF: 0.01 (G)

Chromosome 13:27921083 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs4616145, rs116914624

HGVS names

This variant has 6 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 4 transcripts and has 2506 sample genotypes.

Variant displays