Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

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

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

Most severe consequence
 
Synonymous variant
Evidence status

HGVS names

This variant has 24 HGVS names - Show

Genotyping chips

This variant has assays on 6 chips - Show

About this variant

This variant overlaps 16 transcripts, has 2765 sample genotypes and is mentioned in 1 citation.

Variant displays