Original source

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

Alleles
A/- | Ancestral: A | MAF: 0.30 (A)
Location

Chromosome 1:113865422 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

This variant has 12 HGVS names - click the plus to show

About this variant

This variant overlaps 11 transcripts and has 2508 sample genotypes.

Variant displays