Original source

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

Alleles
T/G | Ancestral: G | Ambiguity code: K | MAF: 0.20 (T)
Location

Chromosome 19:8977341 (forward strand) | View in location tab

Most severe consequence
 
Missense variant
Evidence status

This variant has 4 synonyms - click the plus to show

This variant has 3 HGVS names - click the plus to show

This variant has assays on 11 chips - click the plus to show

About this variant

This variant overlaps 1 transcript, has 4035 sample genotypes and is mentioned in 1 citation.

Variant displays