Original source

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


Chromosome 1: between 236815695 and 236815696 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs200394864, rs112130300

HGVS names

This variant has 12 HGVS names - Show

About this variant

This variant overlaps 12 transcripts and has 10 sample genotypes.

Variant displays