Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

Alleles
T/G | Ancestral: T | Ambiguity code: K | MAF: 0.34 (G)
Location

Chromosome 12:32610540 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59200752, rs17611600

This variation has 10 HGVS names - click the plus to show

This variation has assays on 9 chips - click the plus to show

Variation displays