Original source

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

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

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

Most severe consequence
 
Intron variant
Evidence status

Synonyms

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