Original source

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

Alleles
-/A/C
Location

Chromosome 12: between 21131693 and 21131694 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs143871795

HGVS names

This variant has 12 HGVS names - Show

About this variant

This variant overlaps 12 transcripts.

Variant displays