Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

C/G | Ancestral: C | Ambiguity code: S | MAF: 0.10 (G)

Chromosome 2:227815621 (forward strand) | View in location tab

Most severe consequence
Non coding transcript exon variant
Evidence status


Archive dbSNP rs60930044

This variant has 5 HGVS names - click the plus to show

About this variant

Variant displays