Original source

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

Alleles
G/- | Ancestral: G | MAF: 0.33 (G)
Location

Chromosome 6:166573448 (forward strand) | View in location tab

Co-located

with dbSNP rs199731828 (G/A/T)

Most severe consequence
Evidence status

Synonyms

This variation has 4 HGVS names - click the plus to show

Variation displays