Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y|MAF: 0.02 (T)
Location

Chromosome 19:8959510 (forward strand)|View in location tab

Co-located variants
Most severe consequence
 
Missense variant
Evidence status

Synonyms

Uniprot VAR_056612

HGVS names

This variant has 3 HGVS names - Show

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

This variant overlaps 1 transcript and has 2759 sample genotypes.

Variant displays