Original source

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

Alleles
-/T|MAF: 0.03 (T)
Location

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

Most severe consequence
 
Intron variant
Evidence status

Synonyms

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