Original source

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

Alleles
-/T | MAF: 0.40 (T)
Location

Chromosome 8: between 23058491 and 23058492 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs370466030, rs200849711

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

About this variant

This variant overlaps 4 transcripts and has 2511 individual genotypes.

Variation displays