Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K | MAF: 0.01 (T)
Location

Chromosome 1:158654738 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM930690

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 5 HGVS names - click the plus to show

This variation has assays on 6 chips - click the plus to show

About this variant

This variant overlaps 3 transcripts, has 2506 individual genotypes and is associated with 2 phenotypes.

Variation displays