Original source

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

Alleles
G/A/C|Ancestral: G|Ambiguity code: V|MAF: 0.05 (G)
Location

Chromosome 1:145925876 (forward strand)|View in location tab

Most severe consequence
 
Splice region variant
Evidence status

Clinical significance

Synonyms

Archive dbSNP rs77434912

HGVS names

This variant has 18 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni1-Quad, Illumina_HumanOmni5

About this variant

This variant overlaps 66 transcripts, has 2506 sample genotypes and is associated with 1 phenotype.

Variant displays