Original source

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

Alleles
T/- | Ancestral: T | MAF: 0.22 (T)
Location

Chromosome 1:26734344 (forward strand) | View in location tab

Co-located

with dbSNP rs565410167 (T/C)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs66884206, rs139080747

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

About this variant

This variant overlaps 6 transcripts and has 2505 individual genotypes.

Variation displays