Original source

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

Alleles
-/T
Location

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

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs372207804

This variation has 5 HGVS names - click the plus to show

About this variant

This variant overlaps 11 transcripts and has 1 individual genotype.

Variation displays