Most severe consequence
Missense variant
T/C|Ancestral: T|Ambiguity code: Y|MAF: 0.19 (C)

Chromosome 19:8978096 (forward strand)|View in location tab

Evidence status

HGVS names

This variant has 5 HGVS names - Show


This variant has 2 synonyms - Show

Genotyping chips

This variant has assays on 5 chips - Show

Original source

Variants (including SNPs and indels) imported from dbSNP (release 147)|View in dbSNP

About this variant

This variant overlaps 1 transcript and has 2839 sample genotypes.

Variant displays