Original source

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

-/AT | MAF: 0.06 (AT)

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


with 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