Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M | MAF: 0.40 (C)
Location

Chromosome 1:115030959 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59333805

This variation has 2 HGVS names - click the plus to show

About this variant

This variant overlaps 2 transcripts and has 2510 individual genotypes.

Variation displays