Original source

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

Alleles
G/T | Ancestral: T | Ambiguity code: K | MAF: 0.10 (G)
Location

Chromosome 3:165780114 (forward strand) | View in location tab

Co-located

with dbSNP rs76032544 (G/T), rs79036095 (G/T)

Most severe consequence
Evidence status

Synonyms

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

Variation displays