Original source

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

Alleles
-/T
Location

Chromosome 18: between 42260834 and 42260835 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs368637924, rs144666736

This variation has 2 HGVS names - click the plus to show

Variation displays