This variant has been flagged

Variation has more than 3 different alleles

Original source

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

Alleles
C/A/G/T | Ancestral: C | Ambiguity code: N | MAF: 0.48 (T)
Location

Chromosome 4:73419522 (forward strand) | View in location tab

Most severe consequence
 
Synonymous variant
Evidence status

This variant has 39 HGVS names - click the plus to show

This variant has assays on 6 chips - click the plus to show

About this variant

This variant overlaps 45 transcripts and has 2575 sample genotypes.

Variant displays