Original source

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

-/T | MAF: 0.03 (T)

Chromosome 12: between 43757179 and 43757180 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs370140457, rs369543384

HGVS names

This variant has 10 HGVS names - Show

About this variant

This variant overlaps 21 transcripts and has 2504 sample genotypes.

Variant displays