Original source

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

Alleles
A/C/T | Ancestral: A | Ambiguity code: H | MAF: 0.32 (T)
Location

Chromosome 1:225850913 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs2090083

This variation has 4 HGVS names - click the plus to show

About this variant

This variant overlaps 8 transcripts and has 2508 individual genotypes.

Variation displays