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

Chromosome 7:39024584 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

This variant has 12 HGVS names - click the plus to show

About this variant

This variant overlaps 9 transcripts and has 1 sample genotype.

Variant displays