Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: < 0.01 (T)
Location

Chromosome 19:10154636 (forward strand) | View in location tab

Most severe consequence
 
Synonymous variant
Evidence status

This variant has 8 HGVS names - click the plus to show

This variant has assays on 6 chips - click the plus to show

About this variant

This variant overlaps 8 transcripts, has 2765 sample genotypes and is mentioned in 1 citation.

Variant displays