Original source

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

Alleles
T/C|Ancestral: T|Ambiguity code: Y|MAF: 0.29 (C)
Location

Chromosome 12:130120384 (forward strand)|View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

Synonyms

Archive dbSNP rs59253827, rs386511726

HGVS name

12:g.130120384T>C

Genotyping chips

This variant has assays on 6 chips - Show

About this variant

This variant overlaps 1 transcript, has 4972 sample genotypes and is mentioned in 1 citation.

Variant displays