Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K | MAF: < 0.01 (T)
Location

Chromosome 19:5831880 (forward strand) | View in location tab

Most severe consequence
 
Missense variant
Evidence status

This variant has 3 synonyms - click the plus to show

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

About this variant

This variant overlaps 12 transcripts, has 2810 sample genotypes and is mentioned in 4 citations.

Variant displays