Original source

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

Alleles
G/C | Ancestral: C | Ambiguity code: S | MAF: 0.01 (G)
Location

Chromosome 2:208249074 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs57877504

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

About this variant

This variant overlaps 11 transcripts and has 2679 individual genotypes.

Variation displays