Original source

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

Alleles
-/TTCT
Location

Chromosome 5: between 132301826 and 132301827 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Synonyms

Archive dbSNP rs377052759

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 2 transcripts and has 1 sample genotype.

Variant displays