Original source

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

Alleles
T/A | Ancestral: T | Ambiguity code: W | MAF: 0.28 (A)
Location

Chromosome 12:40320099 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM104616

Most severe consequence
Evidence status

Clinical significance

This variation has 6 synonyms - click the plus to show

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

This variation has assays on 7 chips - click the plus to show

Variation displays