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 7:55200351 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Uniprot VAR_019299

This variation has 12 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_Human1M-duo, Illumina_HumanOmni5

About this variant

This variant overlaps 6 transcripts, has 86 individual genotypes and is mentioned in 2 citations.

Variation displays