Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K
Location

Chromosome 1:58950969 (forward strand) | View in location tab

Most severe consequence
Synonyms

Archive dbSNP rs1238811

This variation has 8 HGVS names - click the plus to show

Variation displays