Original source

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

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

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

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs62383029

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 22 transcripts and has 1 sample genotype.

Variant displays