Original source

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

Alleles
-/T | MAF: 0.28 (T)
Location

Chromosome 1: between 219929526 and 219929527 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs34409360, rs71949445

This variation has 2 HGVS names - click the plus to show

About this variant

This variant overlaps 3 transcripts and has 2506 individual genotypes.

Variation displays