Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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

About this variant

This variant overlaps 9 transcripts and has 2504 individual genotypes.

Variation displays