Original source

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

Alleles
G/-|Ancestral: G|MAF: 0.38 (G)
Location

Chromosome 10:62401487 (forward strand)|View in location tab

Co-located variant

dbSNP rs202164670 (G/T)

Most severe consequence
 
3 prime UTR variant
Evidence status

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 4 transcripts and has 2513 sample genotypes.

Variant displays