Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.12 (C)
Location

Chromosome 1:167282190 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58337723

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

About this variant

This variant overlaps 10 transcripts and has 2510 individual genotypes.

Variation displays