Original source

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

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

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

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 38 HGVS names - Show

About this variant

This variant overlaps 37 transcripts and has 243 sample genotypes.

Variant displays