Original source

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

Alleles
C/G/T|Ancestral: G|Ambiguity code: B|MAF: < 0.01 (A)
Location

Chromosome 1:145925773 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

HGVS names

This variant has 18 HGVS names - Show

About this variant

This variant overlaps 66 transcripts and has 2505 sample genotypes.

Variant displays