Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.03 (T)
Location

Chromosome 9:35092908 (forward strand) | View in location tab

Most severe consequence
 
Non coding transcript exon variant
Evidence status

This variant has 6 HGVS names - click the plus to show

About this variant

This variant overlaps 9 transcripts and has 2504 sample genotypes.

Variant displays