Original source

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

Alleles
A/T | Ancestral: A | Ambiguity code: W
Location

Chromosome 1:114406545 (forward strand) | View in location tab

Co-located

with dbSNP rs369280519 (A/-/AT/ATA)

Most severe consequence
Evidence status

This variation has 12 HGVS names - click the plus to show

Variation displays