Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 7:55143357 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Uniprot VAR_019293

This variation has 20 HGVS names - click the plus to show

This variation has assays on 4 chips - click the plus to show

About this variant

This variant overlaps 9 transcripts, has 833 individual genotypes and is mentioned in 1 citation.

Variation displays