Original source

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

Alleles
G/T|Ancestral: T|Ambiguity code: K|MAF: 0.35 (T)
Location

Chromosome 12:71938143 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CR056785

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs60080807

HGVS name

12:g.71938143G>T

Genotyping chips

This variant has assays on 6 chips - Show

About this variant

This variant overlaps 2 transcripts, has 2581 sample genotypes and is mentioned in 84 citations.

Variant displays