Original source

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

Alleles
-/T | MAF: 0.29 (-)
Location

Chromosome 18: between 44680869 and 44680870 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs368637924, rs144666736

This variant has 2 HGVS names - click the plus to show

About this variant

This variant overlaps 3 transcripts and has 2505 sample genotypes.

Variant displays