Original source

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

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

Chromosome 1:230281625 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs3811483

HGVS names

This variant has 4 HGVS names - Hide

1:g.230281625C>T
ENST00000414640.1:n.269G>A
ENST00000366672.4:c.*2167C>T
ENST00000485438.1:n.3535C>T

Genotyping chips

This variant has assays on 6 chips - Show

About this variant

This variant overlaps 3 transcripts and has 3760 sample genotypes.

Variant displays