Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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

with HGMD-PUBLIC CR068449

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs10373278, rs56657495

This variant has 3 HGVS names - click the plus to show

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

This variant has assays on 6 chips - click the plus to show

About this variant

This variant overlaps 8 transcripts, has 3764 sample genotypes and is mentioned in 42 citations.

Variant displays