Original source

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

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

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

Most severe consequence
Splice region variant
Evidence status

Clinical significance


Archive dbSNP rs77434912

HGVS names

This variant has 14 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni1-Quad, Illumina_HumanOmni5

About this variant

This variant overlaps 64 transcripts, has 2506 sample genotypes and is associated with 1 phenotype.

Variant displays