Original source

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

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

Chromosome 1:145925773 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 6 HGVS names - click the plus to show

About this variant

This variant overlaps 54 transcripts and has 2505 individual genotypes.

Variation displays