Original source

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

Alleles
-/GT/GTGT
Location

Chromosome 18: between 44818993 and 44818994 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs202122294, rs61416824

This variant has 6 HGVS names - click the plus to show

About this variant

This variant overlaps 4 transcripts and has 3 sample genotypes.

Variant displays