Original source

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

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

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