Original source

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

Alleles
C/G | Ambiguity code: S
Location

Chromosome 15:82822408 (forward strand) | View in location tab

Co-located

with dbSNP rs1651959 (C/G)

Most severe consequence

This variation has 10 HGVS names - click the plus to show

Variation displays