Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M | MAF: 0.24 (C)
Location

Chromosome 4:54295646 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs3796765, rs58505840

This variation has 4 HGVS names - click the plus to show

This variation has assays on 6 chips - click the plus to show

About this variant

This variant overlaps 3 transcripts, has 3760 individual genotypes and is mentioned in 1 citation.

Variation displays