Original source

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

Synonyms

Archive dbSNP rs59253827, rs386511726

HGVS name

12:g.130120384T>C

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

About this variant

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

Variation displays