Original source

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

Alleles
-/T
Location

Chromosome 12: between 48770064 and 48770065 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs372207804

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 11 transcripts and has 1 sample genotype.

Variant displays