Original source

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

Alleles
T/- | Ancestral: T
Location

Chromosome 1:186671692 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms
HGVS name

1:g.186671692delT

About this variant

This variant overlaps 4 transcripts and has 90 individual genotypes.

Variation displays