Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.42 (C)
Location

Chromosome 5:136056737 (forward strand) | View in location tab

Most severe consequence
 
Synonymous variant
Evidence status

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

This variant has assays on 9 chips - click the plus to show

About this variant

This variant overlaps 13 transcripts, 1 regulatory feature, has 2650 sample genotypes and is mentioned in 6 citations.

Variant displays