Original source

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

Alleles
G/A | Ambiguity code: R | MAF: 0.14 (T)
Location

Chromosome 1:149033329 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs61804965

This variation has 3 HGVS names - click the plus to show

About this variant

This variant overlaps 13 transcripts and has 2682 individual genotypes.

Variation displays