Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.50 (C)
Location

Chromosome 16:50745428 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

This variant has 13 HGVS names - click the plus to show

About this variant

This variant overlaps 16 transcripts, has 2509 sample genotypes and is mentioned in 1 citation.

Variant displays