Original source

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


Chromosome 4: between 89739139 and 89739140 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs367690065

HGVS names

This variant has 12 HGVS names - Show

About this variant

This variant overlaps 12 transcripts, 1 regulatory feature and has 1 sample genotype.

Variant displays