Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

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

Chromosome 19: between 42085772 and 42085773 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs371276723

HGVS name

19:g.42085772_42085773insT

Variation displays