Original source

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

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.07 (T)
Location

Chromosome 1:219929450 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

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

This variant has assays on 6 chips - click the plus to show

About this variant

This variant overlaps 3 transcripts and has 3273 sample genotypes.

Variant displays