Original source

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

Alleles
C/- | MAF: 0.08 (-)
Location

Chromosome 1:149033371 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 3 HGVS names - click the plus to show

About this variant

This variant overlaps 13 transcripts and has 5 individual genotypes.

Variation displays