Original source

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

Alleles
-/TTCT/TTTC
Location

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

Most severe consequence
 
Intron variant
Synonyms

Archive dbSNP rs377052759

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

About this variant

This variant overlaps 4 transcripts and has 1 sample genotype.

Variant displays