Original source

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

Alleles
G/C | Ancestral: C | Ambiguity code: S | MAF: 0.48 (C)
Location

Chromosome 9:123365221 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 3 HGVS names - click the plus to show

About this variant

This variant overlaps 5 transcripts and has 2509 individual genotypes.

Variation displays