Original source

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

Alleles
T/A | Ambiguity code: W
Location

Chromosome 12:32858117 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs60599101

This variant has 6 HGVS names - click the plus to show

About this variant

This variant overlaps 4 transcripts and has 1 sample genotype.

Variant displays