Original source

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

Alleles
C/G|Ancestral: G|Ambiguity code: S|MAF: 0.24 (G)
Location

Chromosome 19:33386617 (forward strand)|View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

HGVS name

19:g.33386617C>G

About this variant

This variant overlaps 9 transcripts and has 2508 sample genotypes.

Variant displays