Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

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

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

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs17743200, rs60202344

HGVS names

This variant has 22 HGVS names - Show

Genotyping chips

This variant has assays on 4 chips - 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