Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.23 (T)
Location

Chromosome 5:174729165 (forward strand) | View in location tab

Most severe consequence
 
Missense variant
Evidence status

This variant has 5 synonyms - click the plus to show

This variant has 4 HGVS names - click the plus to show

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

About this variant

This variant overlaps 2 transcripts, has 2647 sample genotypes and is mentioned in 3 citations.

Variant displays