Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|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

HGVS names

This variant has 8 HGVS names - Show

About this variant

This variant overlaps 10 transcripts and has 2601 sample genotypes.

Variant displays