Original source

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

Alleles
-/T | MAF: < 0.01 (T)
Location

Chromosome 19: between 42589924 and 42589925 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs371276723

HGVS name

19:g.42589924_42589925insT

Variation displays