Original source

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

Alleles
T/- | Ancestral: T | MAF: 0.23 (T)
Location

Chromosome 1:167384022 (forward strand) | View in location tab

Co-located

with dbSNP rs200716576 (T/A)

Most severe consequence
Evidence status

Synonyms

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

About this variant

This variant overlaps 13 transcripts and has 2514 individual genotypes.

Variation displays