Original source

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

Alleles
G/- | Ancestral: G | MAF: 0.42 (-)
Location

Chromosome 8:93921096 (forward strand) | View in location tab

Co-located

with dbSNP rs201669269 (G/A)

Most severe consequence
 
Intron variant
Evidence status

This variant has 11 HGVS names - click the plus to show

About this variant

This variant overlaps 12 transcripts and has 2511 sample genotypes.

Variant displays