Original source

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

Alleles
G/T | Ancestral: T | Ambiguity code: K | MAF: 0.42 (G)
Location

Chromosome 1:88683110 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs57814975

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

This variant has assays on 12 chips - click the plus to show

About this variant

This variant overlaps 5 transcripts, 1 regulatory feature, has 3968 sample genotypes and is associated with 1 phenotype.

Variant displays