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
T/A/C/G | Ancestral: T | Ambiguity code: N | MAF: 0.45 (G)
Location

Chromosome 15:88859365 (forward strand) | View in location tab

Most severe consequence
 
Synonymous variant
Evidence status

Synonyms

This variant has 21 HGVS names - click the plus to show

This variant has assays on 7 chips - click the plus to show

About this variant

This variant overlaps 18 transcripts and has 5539 sample genotypes.

Variant displays