Original source

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


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

Co-located variant

dbSNP rs113663856 (-/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.

Variant displays