Original source

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

Alleles
C/T|Ancestral: T|Ambiguity code: Y|MAF: 0.15 (C)
Location

Chromosome 22:31206201 (forward strand)|View in location tab

Co-located variant

dbSNP rs56138957 (C/T)

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms
HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 7 transcripts and has 3526 sample genotypes.

Variant displays