Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.21 (T)
Location

Chromosome 1:167285408 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

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

About this variant

This variant overlaps 10 transcripts and has 2510 sample genotypes.

Variant displays