Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
T/G | Ambiguity code: K | MAF: 0.30 (T)
Location

Chromosome 12:21046894 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs57331118

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

This variation has assays on 4 chips - click the plus to show

Variation displays