Original source

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

Alleles
G/C/T | Ancestral: G | Ambiguity code: B | MAF: < 0.01 (C)
Location

Chromosome 9:122202658 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 12 HGVS names - click the plus to show

About this variant

This variant overlaps 23 transcripts and has 2504 individual genotypes.

Variation displays