Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.29 (A)
Location

Chromosome 5:79126136 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM031139

Most severe consequence
Evidence status

This variation has 3 synonyms - click the plus to show

This variation has 9 HGVS names - click the plus to show

This variation has assays on 11 chips - click the plus to show

About this variant

This variant overlaps 6 transcripts, has 2686 individual genotypes and is mentioned in 39 citations.

Variation displays