Original source

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

-/T | MAF: 0.31 (T)

Chromosome 1: between 219929526 and 219929527 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs34409360, rs71949445

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 3 transcripts and has 2506 sample genotypes.

Variant displays