Original source

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

Alleles
T/A | Ancestral: T | Ambiguity code: W
Location

Chromosome 4:154611865 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs3020706

This variation has 17 HGVS names - click the plus to show

About this variant

This variant overlaps 13 transcripts and has 262 individual genotypes.

Variation displays