Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

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

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


with dbSNP rs201669269 (G/A)

Most severe consequence
Evidence status

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

About this variant

This variant overlaps 12 transcripts and has 1102 individual genotypes.

Variation displays