Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.38 (G)
Location

Chromosome 14:100839708 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs17743200, rs60202344

This variant has 22 HGVS names - click the plus to show

This variant has assays on 4 chips - click the plus to show

About this variant

This variant overlaps 23 transcripts, 1 regulatory feature, has 2831 sample genotypes, is associated with 1 phenotype and is mentioned in 5 citations.

Variant displays