Original source

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


Chromosome 1: between 26756565 and 26756566 (forward strand) | View in location tab

Most severe consequence
Intron variant

Archive dbSNP rs66846392, rs66846391

HGVS names

This variant has 7 HGVS names - Show

About this variant

This variant overlaps 5 transcripts and has 1 sample genotype.

Variant displays