This variant has been flagged

Variation has more than 3 different alleles

Original source

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

A/C/G/T | Ancestral: A | Ambiguity code: N

Chromosome 2:104854218 (forward strand) | View in location tab

Most severe consequence
Intron variant
HGVS names

This variant has 6 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 21 transcripts and 1 regulatory feature.

Variant displays