Original source

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

Alleles
T/- | Ancestral: T
Location

Chromosome 1:27703320 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58634000

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

Variation displays