Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S | MAF: 0.11 (G)
Location

Chromosome 4:89772325 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs17796079

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

About this variant

This variant overlaps 11 transcripts, has 3116 individual genotypes and is mentioned in 2 citations.

Variation displays