Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S | MAF: 0.44 (C)
Location

Chromosome 12:21839190 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58283879, rs1688472

This variation has 8 HGVS names - click the plus to show

About this variant

This variant overlaps 6 transcripts and has 2779 individual genotypes.

Variation displays