Original source

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

Alleles
T/A | Ancestral: T | Ambiguity code: W
Location

Chromosome 6:49399012 (forward strand) | View in location tab

Most severe consequence
Synonyms

Archive dbSNP rs3205264

This variation has 2 HGVS names - click the plus to show

Variation displays