Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|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
 
Intron variant
Evidence status

HGVS names

This variant has 14 HGVS names - Show

About this variant

This variant overlaps 17 transcripts and has 2583 sample genotypes.

Variant displays