Original source

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

Alleles
-/GC
Location

Chromosome 12: between 6378571 and 6378572 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Synonyms

This variant has 4 HGVS names - click the plus to show

About this variant

This variant overlaps 18 transcripts.

Variant displays