Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M | MAF: 0.05 (T)
Location

Chromosome 1:145928570 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 18 HGVS names - click the plus to show

About this variant

This variant overlaps 27 transcripts and has 2504 individual genotypes.

Variation displays