Original source

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

HGVS names

This variant has 12 HGVS names - Show

About this variant

This variant overlaps 13 transcripts.

Variant displays