Original source

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

Alleles
A/-/AT/ATA | Ancestral: A
Location

Chromosome 1:113863923 (forward strand) | View in location tab

Co-located

with dbSNP rs66847326 (A/T)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs377767231

This variation has 36 HGVS names - click the plus to show

Variation displays