Original source

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

Alleles
G/C | Ambiguity code: S | MAF: 0.50 (C)
Location

Chromosome 10:133528811 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

This variant has 8 HGVS names - click the plus to show

About this variant

This variant overlaps 10 transcripts and has 2601 sample genotypes.

Variant displays