Original source

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

Alleles
-/AT|MAF: 0.06 (AT)
Location

Chromosome 1: between 77944321 and 77944322 (forward strand)|View in location tab

Co-located variant

dbSNP rs145677257 (-/AT)

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 9 HGVS names - Show

About this variant

This variant overlaps 17 transcripts and has 2505 sample genotypes.

Variant displays