Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.23 (A)
Location

Chromosome 12:130127245 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs57243081, rs59304763

HGVS name

12:g.130127245A>G

This variation has assays on 8 chips - click the plus to show

Variation displays