This variation has been flagged

Variation has more than 3 different alleles

Original source

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

G/A/C/T | Ancestral: G | Ambiguity code: N | MAF: 0.10 (A)

Chromosome 19:33391316 (forward strand) | View in location tab

Most severe consequence
Evidence status


This variation has 21 HGVS names - click the plus to show

This variation has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 21 transcripts, has 3663 individual genotypes and is mentioned in 1 citation.

Variation displays