Original source

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

Alleles
C/A/T | Ancestral: A | Ambiguity code: H | MAF: 0.13 (A)
Location

Chromosome 19:33299630 (forward strand) | View in location tab

Most severe consequence
Evidence status

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

About this variant

This variant overlaps 10 transcripts and has 2504 individual genotypes.

Variation displays