Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.43 (A)
Location

Chromosome 2:127257108 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs57011903, rs52816401

This variation has 2 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad, Illumina_Cardio-Metabo_Chip

About this variant

This variant overlaps 5 transcripts, has 1453 individual genotypes and is mentioned in 1 citation.

Variation displays