Original source

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

Alleles
A/- | Ancestral: A
Location

Chromosome 4:74036811 (forward strand) | View in location tab

Co-located

with dbSNP rs199517714 (A/T)

Most severe consequence

This variation has 2 HGVS names - click the plus to show

Variation displays