Original source

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

Alleles
T/C|Ancestral: C|Ambiguity code: Y|MAF: 0.07 (T)
Location

Chromosome 12:21644660 (forward strand)|View in location tab

Co-located variant

dbSNP rs67185134 (CA/TG)

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs58928713

HGVS names

This variant has 7 HGVS names - Show

About this variant

This variant overlaps 6 transcripts and has 2509 sample genotypes.

Variant displays