Original source

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

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

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

Co-located variant

dbSNP rs201669269 (G/A)

Most severe consequence
Intron variant
Evidence status

HGVS names

This variant has 11 HGVS names - Show

About this variant

This variant overlaps 12 transcripts and has 2511 sample genotypes.

Variant displays