Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.43 (G)
Location

Chromosome 12:10536158 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs2617155, rs17809135

This variation has 19 HGVS names - click the plus to show

Variation displays