Original source

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

C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.19 (T)

Chromosome 22:23280019 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs74277901, rs61362261

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 6 transcripts and has 3024 sample genotypes.

Variant displays