Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 19:5831969 (forward strand) | View in location tab

Most severe consequence
 
Missense variant

This variant has 11 HGVS names - click the plus to show

About this variant

This variant overlaps 12 transcripts.

Variant displays