Original source

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

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

Chromosome 5:159316780 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 2 synonyms - click the plus to show

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, has 2536 individual genotypes and is mentioned in 6 citations.

Variation displays