Original source

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

Alleles
-/A
Location

Chromosome 19: between 10176168 and 10176169 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Synonyms

Archive dbSNP rs376051696

This variant has 12 HGVS names - click the plus to show

About this variant

This variant overlaps 13 transcripts.

Variant displays