Original source

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

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

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

Most severe consequence
Non coding transcript exon variant
Evidence status


Archive dbSNP rs73952908

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 6 transcripts and has 2506 sample genotypes.

Variant displays