Original source

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

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.49 (C)
Location

Chromosome 19:33386843 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

19:g.33386843C>T

This variation has assays on 6 chips - click the plus to show

About this variant

This variant overlaps 9 transcripts and has 3963 individual genotypes.

Variation displays