Original source

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

Alleles
C/T|Ancestral: T|Ambiguity code: Y|MAF: 0.41 (T)
Location

Chromosome 1:12207235 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CR051714

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs3737956

HGVS names

This variant has 3 HGVS names - Show

Genotyping chips

This variant has assays on 6 chips - Show

About this variant

This variant overlaps 2 transcripts, has 3086 sample genotypes and is mentioned in 12 citations.

Variant displays