Original source

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

Alleles
T/A/C | Ancestral: T | Ambiguity code: H | MAF: 0.02 (A)
Location

Chromosome 18:44678682 (forward strand) | View in location tab

Most severe consequence
 
Non coding transcript exon variant
Evidence status

Synonyms

Archive dbSNP rs73952908

This variant has 4 HGVS names - click the plus to show

About this variant

This variant overlaps 6 transcripts and has 2506 sample genotypes.

Variant displays