Original source

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

C/G/T | Ancestral: C | Ambiguity code: B | MAF: 0.50 (C)

Chromosome 4:73419522 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 26 HGVS names - click the plus to show

This variation has assays on 6 chips - click the plus to show

About this variant

This variant overlaps 30 transcripts, has 1176 individual genotypes and is mentioned in 1 citation.

Variation displays