Original source

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

Alleles
T/A/C | Ancestral: T | Ambiguity code: H | MAF: < 0.01 (A)
Location

Chromosome 19:2430373 (forward strand) | View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

This variant has 8 HGVS names - click the plus to show

About this variant

This variant overlaps 20 transcripts and has 2504 sample genotypes.

Variant displays