Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y
Location

Chromosome 5:139272605 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs62383029

This variant has 2 HGVS names - click the plus to show

About this variant

This variant overlaps 22 transcripts and has 1 sample genotype.

Variant displays