Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K | MAF: 0.02 (T)
Location

Chromosome 15:74720646 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM057662

Most severe consequence
Evidence status

This variation has 5 synonyms - click the plus to show

This variation has 13 HGVS names - click the plus to show

This variation has assays on 6 chips - click the plus to show

Variation displays