Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
-/T | MAF: 0.04 (T)
Location

Chromosome 12: between 44150982 and 44150983 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs370140457, rs369543384

This variation has 10 HGVS names - click the plus to show

Variation displays