Original source

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

Alleles
C/G/T | Ancestral: C | Ambiguity code: B | MAF: < 0.01 (G)
Location

Chromosome 19:16478911 (forward strand) | View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

This variant has 4 HGVS names - click the plus to show

About this variant

This variant overlaps 8 transcripts and has 2504 sample genotypes.

Variant displays