Original source

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

Alleles
-/T/TT
Location

Chromosome 7: between 16124107 and 16124108 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms
HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 4 transcripts and has 1 sample genotype.

Variant displays