Original source

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

T/G | Ancestral: G | Ambiguity code: K | MAF: 0.06 (T)

Chromosome 9:34126790 (forward strand) | View in location tab


with dbSNP rs113354924 (T/-)

Most severe consequence
Evidence status


Archive dbSNP rs59474536

This variation has 2 HGVS names - click the plus to show

This variation has assays on 4 chips - click the plus to show

About this variant

This variant overlaps 5 transcripts and has 2218 individual genotypes.

Variation displays