Original source

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

Alleles
A/T | Ancestral: A | Ambiguity code: W | MAF: 0.02 (T)
Location

Chromosome 1:167263573 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 11 HGVS names - click the plus to show

About this variant

This variant overlaps 11 transcripts, has 2504 individual genotypes and is mentioned in 1 citation.

Variation displays