Original source

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

G/T | Ancestral: G | Ambiguity code: K | MAF: 0.34 (T)

Chromosome 3:184373361 (forward strand) | View in location tab


with HGMD-PUBLIC CS014432

Most severe consequence
Evidence status


Archive dbSNP rs60055022

This variation has 6 HGVS names - click the plus to show

This variation has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 13 transcripts and has 2400 individual genotypes.

Variation displays