Original source

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


Chromosome 1: between 113816441 and 113816442 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status

HGVS names

This variant has 8 HGVS names - Show

About this variant

This variant overlaps 15 transcripts and has 2 sample genotypes.

Variant displays