Original source

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

Alleles
-/GC
Location

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

Most severe consequence
 
Intron variant
Synonyms
HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 18 transcripts.

Variant displays