Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S
Location

Chromosome 12:110915715 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Uniprot VAR_029449

This variation has 7 HGVS names - click the plus to show

This variation has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 5 transcripts, has 271 individual genotypes and is mentioned in 1 citation.

Variation displays