Original source

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

Alleles
T/- | Ancestral: T | MAF: 0.01 (-)
Location

Chromosome 1:38509576 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs367571258

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

Variation displays