Original source

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

Alleles
G/T|Ancestral: G|Ambiguity code: K|MAF: 0.42 (G)
Location

Chromosome 1:11021823 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 22 HGVS names - Show

About this variant

This variant overlaps 35 transcripts and has 2778 sample genotypes.

Variant displays