Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
A/C | Ancestral: A | Ambiguity code: M | MAF: < 0.01 (C)
Location

Chromosome 5:140787635 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Uniprot VAR_021872

This variation has 7 HGVS names - click the plus to show

This variation has assays on 7 chips - click the plus to show

About this variant

This variant overlaps 5 transcripts and has 2550 individual genotypes.

Variation displays