Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K
Location

Chromosome 3:165490964 (forward strand) | View in location tab

Most severe consequence
Synonyms

Archive dbSNP rs3181876

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

Variation displays