Original source

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

Alleles
C/A/G|Ancestral: C|Ambiguity code: V|MAF: < 0.01 (A)
Location

Chromosome 5:150121879 (forward strand)|View in location tab

Most severe consequence
 
Splice donor variant
Evidence status

HGVS names

This variant has 10 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_HumanOmni5

About this variant

Variant displays