Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.29 (A)
Location

Chromosome 12:130127245 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs57243081, rs59304763

HGVS name

12:g.130127245A>G

This variation has assays on 8 chips - click the plus to show

About this variant

This variant overlaps 1 transcript, has 4977 individual genotypes and is mentioned in 1 citation.

Variation displays