Original source

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

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

Chromosome 1:55067069 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR065654

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

This variant has 2 HGVS names - click the plus to show

1:g.55067069G>C
ENST00000294383.6:c.*1976C>G

This variant has assays on 4 chips - click the plus to show

About this variant

This variant overlaps 5 transcripts, has 4310 sample genotypes and is mentioned in 4 citations.

Variant displays