Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
C/A|Ambiguity code: M|MAF: 0.38 (C)
Location

Chromosome 19:16478719 (forward strand)|View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 4 transcripts and has 2509 sample genotypes.

Variant displays