Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K | MAF: 0.04 (G)
Location

Chromosome 19:45418539 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 14 HGVS names - click the plus to show

About this variant

This variant overlaps 17 transcripts and has 2583 individual genotypes.

Variation displays