Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y
Location

Chromosome 12:7691879 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs9738569

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

About this variant

This variant overlaps 1 transcript and has 3 sample genotypes.

Variant displays