Original source

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

Alleles
-/C|MAF: 0.24 (-)
Location

Chromosome 18: between 5408276 and 5408277 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs142726137

HGVS names

This variant has 17 HGVS names - Show

About this variant

This variant overlaps 17 transcripts and has 2508 sample genotypes.

Variant displays