Original source

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

Alleles
-/CT/TC
Location

Chromosome 10: between 102064799 and 102064800 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms
HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 4 transcripts and has 7 sample genotypes.

Variant displays