Original source

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

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.01 (T)
Location

Chromosome 7:22729768 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 9 HGVS names - click the plus to show

Variation displays