Original source

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

T/- | Ancestral: T

Chromosome 1:38044596 (forward strand) | View in location tab


with dbSNP rs62676861 (T/G)

Most severe consequence
3 prime UTR variant
Evidence status

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 3 transcripts and 1 regulatory feature.

Variant displays