Original source

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

Alleles
-/C | MAF: 0.27 (C)
Location

Chromosome 19: between 33389497 and 33389498 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

This variant has 5 HGVS names - click the plus to show

About this variant

This variant overlaps 7 transcripts and has 2505 sample genotypes.

Variant displays