Original source

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

T/G | Ancestral: T | Ambiguity code: K

Chromosome 18:55525291 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status

This variant has 38 HGVS names - click the plus to show

About this variant

This variant overlaps 37 transcripts and has 243 sample genotypes.

Variant displays