Original source

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


Chromosome 1: between 230709453 and 230709454 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs397932909, rs72464256

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 2 transcripts and has 1 sample genotype.

Variant displays