Original source

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

Alleles
C/T|Ancestral: T|Ambiguity code: Y|MAF: 0.40 (C)
Location

Chromosome 7:128954671 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CR068449

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs10373278, rs56657495

HGVS names

This variant has 3 HGVS names - Hide

7:g.128954671C>T
ENST00000627585.2:c.*746G>A
ENST00000265388.9:c.*746G>A

Genotyping chips

This variant has assays on 6 chips - Show

About this variant

This variant overlaps 8 transcripts, has 3764 sample genotypes and is mentioned in 44 citations.

Variant displays