Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

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

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