Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

-/T | MAF: 0.40 (T)

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

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs370466030, rs200849711

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 4 transcripts and has 2511 sample genotypes.

Variant displays