Original source

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

Alleles
T/A | Ambiguity code: W | MAF: 0.33 (T)
Location

Chromosome 8:128429315 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs77258034

This variation has 6 HGVS names - click the plus to show

Variation displays