Original source

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

Alleles
A/T | Ancestral: T | Ambiguity code: W | MAF: 0.22 (A)
Location

Chromosome 1:115294436 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

This variant has 5 HGVS names - click the plus to show

About this variant

This variant overlaps 3 transcripts, 1 regulatory feature, has 2900 sample genotypes and is mentioned in 1 citation.

Variant displays