Original source

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

C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.16 (T)

Chromosome 22:50584563 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs59371778

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 17 transcripts and has 2506 sample genotypes.

Variant displays