Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

Alleles
G/T | Ancestral: G | Ambiguity code: K | MAF: 0.11 (G)
Location

Chromosome 6:39723717 (forward strand) | View in location tab

Co-located

with dbSNP rs113644178 (A/C)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58659339

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

Variation displays