Original source

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

G/- | Ancestral: T | MAF: 0.33 (G)

Chromosome 10:119662226 (forward strand) | View in location tab


with dbSNP rs2736423 (G/T)

Most severe consequence

This variation has 5 HGVS names - click the plus to show

About this variant

This variant overlaps 3 transcripts and has 1092 individual genotypes.

Variation displays