Original source

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

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

Chromosome 12:12871099 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM033961

Most severe consequence
Evidence status

This variation has 5 synonyms - click the plus to show

This variation has 7 HGVS names - click the plus to show

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

Variation displays