Original source

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

Alleles
T/A | Ancestral: A | Ambiguity code: W
Location

Chromosome 12:8613557 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs61300882

This variant has 2 HGVS names - click the plus to show

About this variant

This variant overlaps 4 transcripts and has 7 sample genotypes.

Variant displays