Original source

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

with dbSNP rs67185134 (CA/TG)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58928713

This variation has 7 HGVS names - click the plus to show

About this variant

This variant overlaps 6 transcripts and has 2509 individual genotypes.

Variation displays