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

Alleles
G/A/C/T | Ancestral: G | Ambiguity code: N
Location

Chromosome 19:5831959 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

This variation has 18 HGVS names - click the plus to show

About this variant

This variant overlaps 36 transcripts and has 2 individual genotypes.

Variation displays