Original source

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

Alleles
-/A/AA|MAF: 0.35 (-)
Location

Chromosome 1: between 77924361 and 77924362 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 16 HGVS names - Show

About this variant

This variant overlaps 14 transcripts and has 2510 sample genotypes.

Variant displays