Original source

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


Chromosome 1: between 26714429 and 26714430 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs397979729

HGVS names

This variant has 10 HGVS names - Show

About this variant

This variant overlaps 6 transcripts and has 2 sample genotypes.

Variant displays