Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
-/G
Location

Chromosome 10: between 112961256 and 112961257 (forward strand) | View in location tab

Most severe consequence
 
Intron variant

This variant has 16 HGVS names - click the plus to show

About this variant

This variant overlaps 15 transcripts.

Variant displays