Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.48 (A)
Location

Chromosome 1:40089945 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs16826396, rs3174871

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

This variation has assays on 5 chips - click the plus to show

Variation displays