Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K | MAF: 0.09 (T)
Location

Chromosome 19:45864964 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs57851804

This variation has 3 HGVS names - click the plus to show

About this variant

This variant overlaps 11 transcripts and has 2554 individual genotypes.

Variation displays