Original source

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

Alleles
T/A | Ancestral: T | Ambiguity code: W | MAF: 0.26 (A)
Location

Chromosome 12:112241552 (forward strand) | View in location tab

Co-located

with dbSNP rs377262633 (T/-)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59102273

This variation has 5 HGVS names - click the plus to show

Variation displays