Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S | MAF: 0.09 (G)
Location

Chromosome 1:115287840 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs3730214, rs61346559

This variation has 5 HGVS names - click the plus to show

About this variant

This variant overlaps 3 transcripts and has 2893 individual genotypes.

Variation displays