Original source

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

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

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

Co-located

with dbSNP rs202164670 (G/T)

Most severe consequence
 
3 prime UTR variant
Evidence status

This variant has 5 HGVS names - click the plus to show

About this variant

This variant overlaps 4 transcripts and has 2513 sample genotypes.

Variant displays