Original source

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

C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.04 (T)

Chromosome 14:99686691 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs74085319

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 4 transcripts and has 2506 sample genotypes.

Variant displays