Original source

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

Alleles
T/-|Ancestral: T
Location

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

Co-located variant

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